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rs797045291

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045291(-;C)
Make rs797045291(C;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position25007221
GeneARX
is asnp
is mentioned by
dbSNPrs797045291
ClinGenrs797045291
ebirs797045291
HLIrs797045291
Exacrs797045291
Varsomers797045291
Maprs797045291
PheGenIrs797045291
hapmaprs797045291
1000 genomesrs797045291
hgdprs797045291
ensemblrs797045291
gopubmedrs797045291
geneviewrs797045291
scholarrs797045291
googlers797045291
pharmgkbrs797045291
gwascentralrs797045291
openSNPrs797045291
23andMers797045291
23andMe allrs797045291
SNP Nexus

SNPshotrs797045291
SNPdbers797045291
MSV3drs797045291
GWAS Ctlgrs797045291
Max Magnitude0
ClinVar
Risk rs797045291(C;C)
Alt rs797045291(C;C)
Reference Rs797045291(;)
Significance Pathogenic
Disease Lissencephaly 2
Variation info
Gene ARX
CLNDBN Lissencephaly 2, X-linked
Reversed 1
HGVS NC_000023.10:g.25025339dupG
CLNSRC
CLNACC RCV000193341.1,