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rs587783202

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783202(-;-)
Make rs587783202(-;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position25013378
GeneARX
is asnp
is mentioned by
dbSNPrs587783202
ebirs587783202
HLIrs587783202
Exacrs587783202
Varsomers587783202
Maprs587783202
PheGenIrs587783202
hapmaprs587783202
1000 genomesrs587783202
hgdprs587783202
ensemblrs587783202
gopubmedrs587783202
geneviewrs587783202
scholarrs587783202
googlers587783202
pharmgkbrs587783202
gwascentralrs587783202
openSNPrs587783202
23andMers587783202
23andMe allrs587783202
SNP Nexus

SNPshotrs587783202
SNPdbers587783202
MSV3drs587783202
GWAS Ctlgrs587783202
Max Magnitude0
ClinVar
Risk rs587783202(;)
Alt rs587783202(;)
Reference rs587783202(G;G)
Significance Pathogenic
Disease Lissencephaly 2
Variation info
Gene ARX
CLNDBN Lissencephaly 2, X-linked
Reversed 1
HGVS NC_000023.10:g.25031495delC
CLNSRC
CLNACC RCV000145058.1,