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rs876657692

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657692(A;A)
Make rs876657692(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position3586681
GeneGIPC3
is asnp
is mentioned by
dbSNPrs876657692
ebirs876657692
HLIrs876657692
Exacrs876657692
Varsomers876657692
Maprs876657692
PheGenIrs876657692
hapmaprs876657692
1000 genomesrs876657692
hgdprs876657692
ensemblrs876657692
gopubmedrs876657692
geneviewrs876657692
scholarrs876657692
googlers876657692
pharmgkbrs876657692
gwascentralrs876657692
openSNPrs876657692
23andMers876657692
23andMe allrs876657692
SNP Nexus

SNPshotrs876657692
SNPdbers876657692
MSV3drs876657692
GWAS Ctlgrs876657692
Max Magnitude0
ClinVar
Risk rs876657692(A;A)
Alt rs876657692(A;A)
Reference rs876657692(G;G)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene GIPC3
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000019.9:g.3586679G>A
CLNSRC
CLNACC RCV000219624.1,