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rs886043552

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position25013205
GeneARX
is asnp
is mentioned by
dbSNPrs886043552
dbSNP (classic)rs886043552
ClinGenrs886043552
ebirs886043552
HLIrs886043552
Exacrs886043552
Gnomadrs886043552
Varsomers886043552
LitVarrs886043552
Maprs886043552
PheGenIrs886043552
Biobankrs886043552
1000 genomesrs886043552
hgdprs886043552
ensemblrs886043552
geneviewrs886043552
scholarrs886043552
googlers886043552
pharmgkbrs886043552
gwascentralrs886043552
openSNPrs886043552
23andMers886043552
23andMe allrs886043552
SNPshotrs886043552
SNPdbers886043552
MSV3drs886043552
GWAS Ctlgrs886043552
Max Magnitude0
ClinVar
Risk rs886043552(-;-)
Alt rs886043552(-;-)
Reference Rs886043552(G;G)
Significance Pathogenic
Disease Lissencephaly 2
Variation info
Gene ARX
CLNDBN Lissencephaly 2, X-linked
Reversed 0
HGVS NC_000023.10:g.25031322delG
CLNSRC
CLNACC RCV000376192.1,