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rs587783183

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783183(A;A)
Make rs587783183(A;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position25007438
GeneARX
is asnp
is mentioned by
dbSNPrs587783183
ebirs587783183
HLIrs587783183
Exacrs587783183
Varsomers587783183
Maprs587783183
PheGenIrs587783183
hapmaprs587783183
1000 genomesrs587783183
hgdprs587783183
ensemblrs587783183
gopubmedrs587783183
geneviewrs587783183
scholarrs587783183
googlers587783183
pharmgkbrs587783183
gwascentralrs587783183
openSNPrs587783183
23andMers587783183
23andMe allrs587783183
SNP Nexus

SNPshotrs587783183
SNPdbers587783183
MSV3drs587783183
GWAS Ctlgrs587783183
Max Magnitude0
ClinVar
Risk rs587783183(A;A)
Alt rs587783183(A;A)
Reference rs587783183(T;T)
Significance Probable-Pathogenic
Disease Lissencephaly 2
Variation info
Gene ARX
CLNDBN Lissencephaly 2, X-linked
Reversed 1
HGVS NC_000023.10:g.25025555A>T
CLNSRC
CLNACC RCV000145039.1,