Variants with conflicting interpretations "affects" and "likely benign"

Submission 1 (affects) minimum review status:		Submission 1 (affects) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Show significances as they were submitted (without aggregation into standard terms)

Total variants with conflicting interpretations: 11

HGVS	dbSNP	gnomAD frequency
NM_004827.3(ABCG2):c.34G>A (p.Val12Met)	rs2231137	0.07814
NM_002386.4(MC1R):c.451C>T (p.Arg151Cys)	rs1805007	0.04832
NM_002386.4(MC1R):c.478C>T (p.Arg160Trp)	rs1805008	0.04620
UGT1A1*6	rs4148323	0.01140
NM_001142864.4(PIEZO1):c.6734G>A (p.Arg2245Gln)	rs2290901	0.01007
NM_005689.4(ABCB6):c.574C>T (p.Arg192Trp)	rs149202834	0.00159
NM_001142864.4(PIEZO1):c.7180G>A (p.Gly2394Ser)	rs201950081	0.00109
NM_000342.4(SLC4A1):c.1972G>A (p.Glu658Lys)	rs75731670	0.00023
NM_001735.3(C5):c.2654G>A (p.Arg885His)	rs56040400	0.00011
NM_001211.6(BUB1B):c.2441G>A (p.Arg814His)	rs28989182	0.00001
NM_025137.4(SPG11):c.833A>G (p.Asn278Ser)	rs75309308

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. The submitted information has not been verified. If you have questions about the information contained on this website, please see a health care professional.