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rs587777876

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777876(C;T)
Make rs587777876(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position71223784
GeneGJB1
is asnp
is mentioned by
dbSNPrs587777876
ebirs587777876
HLIrs587777876
Exacrs587777876
Varsomers587777876
Maprs587777876
PheGenIrs587777876
hapmaprs587777876
1000 genomesrs587777876
hgdprs587777876
ensemblrs587777876
gopubmedrs587777876
geneviewrs587777876
scholarrs587777876
googlers587777876
pharmgkbrs587777876
gwascentralrs587777876
openSNPrs587777876
23andMers587777876
23andMe allrs587777876
SNP Nexus

SNPshotrs587777876
SNPdbers587777876
MSV3drs587777876
GWAS Ctlgrs587777876
Max Magnitude0
ClinVar
Risk rs587777876(T;T)
Alt rs587777876(T;T)
Reference rs587777876(C;C)
Significance Pathogenic
Disease X-linked hereditary motor and sensory neuropathy
Variation info
Gene GJB1
CLNDBN X-linked hereditary motor and sensory neuropathy
Reversed 0
HGVS NC_000023.10:g.70443634C>T
CLNSRC
CLNACC RCV000143795.1,