rs766753922

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs766753922(-;-)

Make rs766753922(-;G)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

80239362

Gene

OTOGL

is a	snp
is	mentioned by
dbSNP	rs766753922
dbSNP (classic)	rs766753922
ClinGen	rs766753922
ebi	rs766753922
HLI	rs766753922
Exac	rs766753922
Gnomad	rs766753922
Varsome	rs766753922
LitVar	rs766753922
Map	rs766753922
PheGenI	rs766753922
Biobank	rs766753922
1000 genomes	rs766753922
hgdp	rs766753922
ensembl	rs766753922
geneview	rs766753922
scholar	rs766753922
google	rs766753922
pharmgkb	rs766753922
gwascentral	rs766753922
openSNP	rs766753922
23andMe	rs766753922
SNPshot	rs766753922
SNPdbe	rs766753922
MSV3d	rs766753922
GWAS Ctlg	rs766753922

Max Magnitude

0

ClinVar
Risk	rs766753922(-;-)
Alt	rs766753922(-;-)
Reference	Rs766753922(G;G)
Significance	Pathogenic
Disease	Nonsyndromic hearing loss and deafness
Variation	info
Gene	OTOGL
CLNDBN	Nonsyndromic hearing loss and deafness
Reversed	0
HGVS	NC_000012.11:g.80633142delG
CLNSRC
CLNACC	RCV000219678.1,