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rs876661269

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876661269(C;C)
Make rs876661269(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position71223858
GeneGJB1
is asnp
is mentioned by
dbSNPrs876661269
ebirs876661269
HLIrs876661269
Exacrs876661269
Varsomers876661269
Maprs876661269
PheGenIrs876661269
hapmaprs876661269
1000 genomesrs876661269
hgdprs876661269
ensemblrs876661269
gopubmedrs876661269
geneviewrs876661269
scholarrs876661269
googlers876661269
pharmgkbrs876661269
gwascentralrs876661269
openSNPrs876661269
23andMers876661269
23andMe allrs876661269
SNP Nexus

SNPshotrs876661269
SNPdbers876661269
MSV3drs876661269
GWAS Ctlgrs876661269
Max Magnitude0
ClinVar
Risk rs876661269(C;C)
Alt rs876661269(C;C)
Reference rs876661269(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GJB1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.70443708T>C
CLNSRC
CLNACC RCV000220727.1,