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rs766753922

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs766753922(-;-)
Make rs766753922(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position80239362
GeneOTOGL
is asnp
is mentioned by
dbSNPrs766753922
ebirs766753922
HLIrs766753922
Exacrs766753922
Varsomers766753922
Maprs766753922
PheGenIrs766753922
hapmaprs766753922
1000 genomesrs766753922
hgdprs766753922
ensemblrs766753922
gopubmedrs766753922
geneviewrs766753922
scholarrs766753922
googlers766753922
pharmgkbrs766753922
gwascentralrs766753922
openSNPrs766753922
23andMers766753922
23andMe allrs766753922
SNP Nexus

SNPshotrs766753922
SNPdbers766753922
MSV3drs766753922
GWAS Ctlgrs766753922
Max Magnitude0
ClinVar
Risk rs766753922(;)
Alt rs766753922(;)
Reference rs766753922(G;G)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene OTOGL
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000012.11:g.80633142delG
CLNSRC
CLNACC RCV000219678.1,