Have questions? Visit https://www.reddit.com/r/SNPedia

rs876661252

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876661252(A;A)
Make rs876661252(A;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position71224249
GeneGJB1
is asnp
is mentioned by
dbSNPrs876661252
ebirs876661252
HLIrs876661252
Exacrs876661252
Varsomers876661252
Maprs876661252
PheGenIrs876661252
hapmaprs876661252
1000 genomesrs876661252
hgdprs876661252
ensemblrs876661252
gopubmedrs876661252
geneviewrs876661252
scholarrs876661252
googlers876661252
pharmgkbrs876661252
gwascentralrs876661252
openSNPrs876661252
23andMers876661252
23andMe allrs876661252
SNP Nexus

SNPshotrs876661252
SNPdbers876661252
MSV3drs876661252
GWAS Ctlgrs876661252
Max Magnitude0
ClinVar
Risk rs876661252(A;A)
Alt rs876661252(A;A)
Reference rs876661252(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GJB1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.70444099T>A
CLNSRC
CLNACC RCV000214039.1,