ClinVar Miner

Variants from Clinical Genomics, Uppaluri K&H Personalized Medicine Clinic

Location: India  Primary collection method: research
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign association association not found drug response total
72 333 1201 306 684 9 1 2 2591

Gene and significance breakdown #

Total genes and gene combinations: 58
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign association association not found drug response total
ABCC8 0 1 457 0 14 1 0 0 465
WFS1 14 44 111 56 234 0 0 0 459
GCK 14 97 72 17 80 0 0 0 280
HNF1A 28 72 49 24 70 0 0 0 240
HNF4A 2 23 60 31 114 0 0 0 230
KCNJ11 0 10 171 3 20 1 1 2 205
HNF1B 13 31 40 44 23 0 0 0 151
TGFBR2 1 4 43 48 0 0 0 0 96
HADH 0 15 17 23 13 0 0 0 68
INS, INS-IGF2 0 15 28 5 16 1 0 0 65
ALMS1 0 1 32 5 10 0 0 0 48
C12orf43, HNF1A 0 1 3 2 23 1 0 0 30
INSR 0 0 7 18 1 0 0 0 26
BLK 0 2 1 2 16 1 0 0 22
GLIS3 0 0 6 2 10 0 0 0 18
HNF1B, LOC126862549 0 4 5 4 2 0 0 0 15
LMNA 0 3 7 3 2 0 0 0 15
DCAF17 0 0 2 1 9 0 0 0 12
ABCC8, LOC110121471 0 0 11 0 3 0 0 0 11
DRD4 0 0 11 0 0 0 0 0 11
PDX1 0 0 9 1 1 0 0 0 11
HADH, LOC129992931 0 0 2 6 2 0 0 0 10
LOC129992166, WFS1 0 0 0 2 8 0 0 0 10
BSCL2, HNRNPUL2-BSCL2 0 0 7 0 0 0 0 0 7
FOXP3 0 3 2 1 1 0 0 0 7
GATA6 0 0 5 0 1 0 0 0 6
IL36RN 0 0 6 0 0 0 0 0 6
AGPAT2 0 1 4 0 0 0 0 0 5
LOC129936399, TGFBR2 0 0 2 3 0 0 0 0 5
BAIAP2 0 0 4 0 0 0 0 0 4
AKT2 0 0 2 1 0 0 0 0 3
ALMS1, LOC126806252 0 2 1 0 0 0 0 0 3
AVP 0 0 3 0 0 0 0 0 3
CARD14 0 0 2 0 0 1 0 0 3
CARD14, SGSH 0 0 3 0 0 0 0 0 3
ENPP1 0 0 2 0 1 0 0 0 3
INS 0 0 1 2 0 0 0 0 3
PAX4 0 0 2 0 1 0 0 0 3
SLC2A2 0 0 1 0 2 0 0 0 3
BLK, LOC126860303 0 0 0 0 2 0 0 0 2
CARD14, LOC126862662, SGSH 0 1 0 0 0 1 0 0 2
DRD5, SLC2A9 0 0 2 0 0 0 0 0 2
GATA4 0 0 1 1 0 0 0 0 2
INS, TH 0 0 0 0 2 0 0 0 2
PTF1A 0 0 2 0 0 0 0 0 2
ZFP57 0 0 1 0 1 0 0 0 2
ABCC8, KCNJ11 0 0 1 0 0 0 0 0 1
ACADS 0 1 0 0 0 0 0 0 1
CEL 0 0 0 0 1 0 0 0 1
HNF4A, R3HDML 0 0 0 0 1 0 0 0 1
KLF11 0 1 0 0 0 0 0 0 1
LMNA, LOC126805877 0 0 0 1 0 0 0 0 1
NEUROD1 0 0 1 0 0 0 0 0 1
PAX6 0 0 1 0 0 0 0 0 1
PCSK9 0 0 0 0 0 1 0 0 1
SLC29A3 0 0 0 0 0 1 0 0 1
TH 0 0 1 0 0 0 0 0 1
TP53 0 1 0 0 0 0 0 0 1

Condition and significance breakdown #

Total conditions: 56
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Condition pathogenic likely pathogenic uncertain significance likely benign benign association association not found drug response total
Maturity-onset diabetes of the young 56 225 830 123 325 0 0 0 1559
Transitory neonatal diabetes mellitus 0 2 444 3 18 0 0 0 467
Wolfram syndrome 1 14 44 110 58 239 0 0 0 465
Diabetic retinopathy 1 4 45 51 0 0 0 0 101
Hyperinsulinemic hypoglycemia 0 12 19 24 15 0 0 0 70
Alstrom syndrome 0 3 33 5 10 0 0 0 51
Type 2 diabetes mellitus 0 8 18 2 16 2 1 0 47
Neonatal insulin-dependent diabetes mellitus 0 5 8 5 18 0 0 0 36
Hyperinsulinism due to INSR deficiency 0 0 6 18 1 0 0 0 25
Systemic lupus erythematosus 0 2 1 2 18 1 0 0 24
Diabetes mellitus, permanent neonatal 4 0 7 12 2 0 0 0 0 21
Neonatal diabetes mellitus 0 1 17 0 0 0 0 0 18
Hereditary attention deficit-hyperactivity disorder 0 0 12 0 0 0 0 0 12
Woodhouse-Sakati syndrome 0 0 2 1 9 0 0 0 12
Hyperinsulinemia 0 0 11 0 0 0 0 0 11
Pancreatic hypoplasia 0 0 9 1 1 0 0 0 11
Dilated cardiomyopathy 1A 0 2 3 3 0 0 0 0 8
Hyperinsulinemic hypoglycemia, familial, 4 0 3 0 4 1 0 0 0 8
Pityriasis rubra pilaris 0 1 5 0 0 2 0 0 8
Congenital generalized lipodystrophy type 2 0 0 7 0 0 0 0 0 7
Hyperinsulinemic hypoglycemia, familial, 1 0 1 5 1 0 0 0 0 7
Insulin-dependent diabetes mellitus secretory diarrhea syndrome 0 3 2 1 1 0 0 0 7
Maturity-onset diabetes of the young type 10 0 1 6 0 0 0 0 0 7
Neonatal hypoglycemia 0 0 3 0 4 0 0 0 7
Primary dilated cardiomyopathy 0 1 4 0 2 0 0 0 7
Acrodermatitis continua suppurativa of Hallopeau 0 0 6 0 0 0 0 0 6
Diabetes mellitus 1 0 0 0 5 0 0 0 6
Congenital generalized lipodystrophy type 1 0 1 4 0 0 0 0 0 5
Neonatal diabetes mellitus with congenital hypothyroidism 0 0 5 0 0 0 0 0 5
Attention deficit hyperactivity disorder 0 0 4 0 0 0 0 0 4
Pancreatic hypoplasia-diabetes-congenital heart disease syndrome 0 0 4 0 0 0 0 0 4
Diabetes mellitus type 1 0 1 2 0 0 0 0 0 3
Diabetes mellitus, transient neonatal, 2 0 0 3 0 0 0 0 0 3
Hyperproinsulinemia 0 0 3 0 0 0 0 0 3
Maturity-onset diabetes of the young type 13 0 0 1 2 0 0 0 0 3
Neurohypophyseal diabetes insipidus 0 0 3 0 0 0 0 0 3
Hypoglycemia 0 2 0 0 0 0 0 0 2
Hypoinsulinemia 0 0 1 0 0 1 0 0 2
Maturity-onset diabetes of the young type 3 0 2 0 0 0 0 0 0 2
Abnormality of refraction 0 0 1 0 0 0 0 0 1
Acanthosis nigricans 0 0 0 0 0 1 0 0 1
Cerebral edema 0 0 1 0 0 0 0 0 1
Deficiency of butyryl-CoA dehydrogenase 0 1 0 0 0 0 0 0 1
Familial hypercholesterolemia 0 0 0 0 0 1 0 0 1
Gastric cancer 0 1 0 0 0 0 0 0 1
Generalized dystonia 0 0 1 0 0 0 0 0 1
Gestational diabetes 0 0 0 0 0 1 0 0 1
Glibenclamide response 0 0 0 0 0 0 0 1 1
Glycosuria 0 0 0 0 1 0 0 0 1
Insulin-resistant diabetes mellitus 0 0 1 0 0 0 0 0 1
Maturity-onset diabetes of the young type 2 0 1 0 0 0 0 0 0 1
Pancreatic beta cell agenesis with neonatal diabetes mellitus 0 0 1 0 0 0 0 0 1
Schizophrenia; Hereditary attention deficit-hyperactivity disorder 0 0 1 0 0 0 0 0 1
Sensorineural hearing loss disorder 0 0 0 0 1 0 0 0 1
Type 1 diabetes mellitus 2 0 1 0 0 0 0 0 0 1
sulfonylureas response 0 0 0 0 0 0 0 1 1

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