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rs587777877

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777877(C;G)
Make rs587777877(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position71223966
GeneGJB1
is asnp
is mentioned by
dbSNPrs587777877
ebirs587777877
HLIrs587777877
Exacrs587777877
Varsomers587777877
Maprs587777877
PheGenIrs587777877
hapmaprs587777877
1000 genomesrs587777877
hgdprs587777877
ensemblrs587777877
gopubmedrs587777877
geneviewrs587777877
scholarrs587777877
googlers587777877
pharmgkbrs587777877
gwascentralrs587777877
openSNPrs587777877
23andMers587777877
23andMe allrs587777877
SNP Nexus

SNPshotrs587777877
SNPdbers587777877
MSV3drs587777877
GWAS Ctlgrs587777877
Max Magnitude0
ClinVar
Risk rs587777877(G;G)
Alt rs587777877(G;G)
Reference rs587777877(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.70443816C>G
CLNSRC
CLNACC RCV000143793.1,