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rs587783096

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783096(A;A)
Make rs587783096(A;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position25007418
GeneARX
is asnp
is mentioned by
dbSNPrs587783096
ebirs587783096
HLIrs587783096
Exacrs587783096
Varsomers587783096
Maprs587783096
PheGenIrs587783096
hapmaprs587783096
1000 genomesrs587783096
hgdprs587783096
ensemblrs587783096
gopubmedrs587783096
geneviewrs587783096
scholarrs587783096
googlers587783096
pharmgkbrs587783096
gwascentralrs587783096
openSNPrs587783096
23andMers587783096
23andMe allrs587783096
SNP Nexus

SNPshotrs587783096
SNPdbers587783096
MSV3drs587783096
GWAS Ctlgrs587783096
Max Magnitude0
ClinVar
Risk rs587783096(A;A)
Alt rs587783096(A;A)
Reference rs587783096(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ARX
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.25025535C>T
CLNSRC
CLNACC RCV000144762.2,