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rs587783184

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783184(A;A)
Make rs587783184(A;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position25007425
GeneARX
is asnp
is mentioned by
dbSNPrs587783184
ebirs587783184
HLIrs587783184
Exacrs587783184
Varsomers587783184
Maprs587783184
PheGenIrs587783184
hapmaprs587783184
1000 genomesrs587783184
hgdprs587783184
ensemblrs587783184
gopubmedrs587783184
geneviewrs587783184
scholarrs587783184
googlers587783184
pharmgkbrs587783184
gwascentralrs587783184
openSNPrs587783184
23andMers587783184
23andMe allrs587783184
SNP Nexus

SNPshotrs587783184
SNPdbers587783184
MSV3drs587783184
GWAS Ctlgrs587783184
Max Magnitude0
ClinVar
Risk rs587783184(A;A)
Alt rs587783184(A;A)
Reference rs587783184(C;C)
Significance Probable-Pathogenic
Disease Lissencephaly 2
Variation info
Gene ARX
CLNDBN Lissencephaly 2, X-linked
Reversed 1
HGVS NC_000023.10:g.25025542G>T
CLNSRC
CLNACC RCV000145040.1,