List of variants in gene RBBP8 reported as likely benign for Jawad syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_002894.3(RBBP8):c.736C>G (p.Pro246Ala)	rs34372414	0.00661
NM_002894.3(RBBP8):c.2024C>T (p.Thr675Ile)	rs186820592	0.00005
NM_002894.3(RBBP8):c.1223_1228del (p.Ile408_Asn409del)	rs757747543

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