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rs587783193

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783193(-;-)
Make rs587783193(-;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position25015566
GeneARX
is asnp
is mentioned by
dbSNPrs587783193
ebirs587783193
HLIrs587783193
Exacrs587783193
Varsomers587783193
Maprs587783193
PheGenIrs587783193
hapmaprs587783193
1000 genomesrs587783193
hgdprs587783193
ensemblrs587783193
gopubmedrs587783193
geneviewrs587783193
scholarrs587783193
googlers587783193
pharmgkbrs587783193
gwascentralrs587783193
openSNPrs587783193
23andMers587783193
23andMe allrs587783193
SNP Nexus

SNPshotrs587783193
SNPdbers587783193
MSV3drs587783193
GWAS Ctlgrs587783193
Max Magnitude0
ClinVar
Risk rs587783193(;)
Alt rs587783193(;)
Reference rs587783193(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ARX
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.25033683delC
CLNSRC
CLNACC RCV000145049.1,