Have questions? Visit https://www.reddit.com/r/SNPedia

rs587783187

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783187(-;-)
Make rs587783187(-;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position25007187
GeneARX
is asnp
is mentioned by
dbSNPrs587783187
ebirs587783187
HLIrs587783187
Exacrs587783187
Varsomers587783187
Maprs587783187
PheGenIrs587783187
hapmaprs587783187
1000 genomesrs587783187
hgdprs587783187
ensemblrs587783187
gopubmedrs587783187
geneviewrs587783187
scholarrs587783187
googlers587783187
pharmgkbrs587783187
gwascentralrs587783187
openSNPrs587783187
23andMers587783187
23andMe allrs587783187
SNP Nexus

SNPshotrs587783187
SNPdbers587783187
MSV3drs587783187
GWAS Ctlgrs587783187
Max Magnitude0
ClinVar
Risk rs587783187(;)
Alt rs587783187(;)
Reference rs587783187(G;G)
Significance Pathogenic
Disease Lissencephaly 2
Variation info
Gene ARX
CLNDBN Lissencephaly 2, X-linked
Reversed 1
HGVS NC_000023.10:g.25025304delC
CLNSRC
CLNACC RCV000145043.1,