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rs267606666

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606666(G;T)
Make rs267606666(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position25013763
GeneARX
is asnp
is mentioned by
dbSNPrs267606666
ebirs267606666
HLIrs267606666
Exacrs267606666
Varsomers267606666
Maprs267606666
PheGenIrs267606666
hapmaprs267606666
1000 genomesrs267606666
hgdprs267606666
ensemblrs267606666
gopubmedrs267606666
geneviewrs267606666
scholarrs267606666
googlers267606666
pharmgkbrs267606666
gwascentralrs267606666
openSNPrs267606666
23andMers267606666
23andMe allrs267606666
SNP Nexus

SNPshotrs267606666
SNPdbers267606666
MSV3drs267606666
GWAS Ctlgrs267606666
Max Magnitude0
ClinVar
Risk rs267606666(T;T)
Alt rs267606666(T;T)
Reference rs267606666(G;G)
Significance Pathogenic
Disease Lissencephaly 2
Variation info
Gene ARX
CLNDBN Lissencephaly 2, X-linked
Reversed 1
HGVS NC_000023.10:g.25031880C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011956.8,