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rs587783182

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783182(C;T)
Make rs587783182(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position25010268
GeneARX
is asnp
is mentioned by
dbSNPrs587783182
ebirs587783182
HLIrs587783182
Exacrs587783182
Varsomers587783182
Maprs587783182
PheGenIrs587783182
hapmaprs587783182
1000 genomesrs587783182
hgdprs587783182
ensemblrs587783182
gopubmedrs587783182
geneviewrs587783182
scholarrs587783182
googlers587783182
pharmgkbrs587783182
gwascentralrs587783182
openSNPrs587783182
23andMers587783182
23andMe allrs587783182
SNP Nexus

SNPshotrs587783182
SNPdbers587783182
MSV3drs587783182
GWAS Ctlgrs587783182
Max Magnitude0
ClinVar
Risk rs587783182(T;T)
Alt rs587783182(T;T)
Reference rs587783182(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ARX
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.25028385G>A
CLNSRC
CLNACC RCV000145038.1,