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rs876661143

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876661143(C;G)
Make rs876661143(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position71223948
GeneGJB1
is asnp
is mentioned by
dbSNPrs876661143
ebirs876661143
HLIrs876661143
Exacrs876661143
Varsomers876661143
Maprs876661143
PheGenIrs876661143
hapmaprs876661143
1000 genomesrs876661143
hgdprs876661143
ensemblrs876661143
gopubmedrs876661143
geneviewrs876661143
scholarrs876661143
googlers876661143
pharmgkbrs876661143
gwascentralrs876661143
openSNPrs876661143
23andMers876661143
23andMe allrs876661143
SNP Nexus

SNPshotrs876661143
SNPdbers876661143
MSV3drs876661143
GWAS Ctlgrs876661143
Max Magnitude0
ClinVar
Risk rs876661143(G;G)
Alt rs876661143(G;G)
Reference rs876661143(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GJB1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.70443798C>G
CLNSRC
CLNACC RCV000218526.1,