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rs876661119

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661119(C;C)
Make rs876661119(C;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position71224079
GeneGJB1
is asnp
is mentioned by
dbSNPrs876661119
ebirs876661119
HLIrs876661119
Exacrs876661119
Varsomers876661119
Maprs876661119
PheGenIrs876661119
hapmaprs876661119
1000 genomesrs876661119
hgdprs876661119
ensemblrs876661119
gopubmedrs876661119
geneviewrs876661119
scholarrs876661119
googlers876661119
pharmgkbrs876661119
gwascentralrs876661119
openSNPrs876661119
23andMers876661119
23andMe allrs876661119
SNP Nexus

SNPshotrs876661119
SNPdbers876661119
MSV3drs876661119
GWAS Ctlgrs876661119
Max Magnitude0
ClinVar
Risk rs876661119(C;C)
Alt rs876661119(C;C)
Reference rs876661119(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GJB1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.70443929G>C
CLNSRC
CLNACC RCV000216227.1,