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

rs797045289

From SNPedia

Orientationminus
Make rs797045289(-;-)
Make rs797045289(-;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position25010283
GeneARX
is asnp
is mentioned by
dbSNPrs797045289
ebirs797045289
HLIrs797045289
Exacrs797045289
Varsomers797045289
Maprs797045289
PheGenIrs797045289
hapmaprs797045289
1000 genomesrs797045289
hgdprs797045289
ensemblrs797045289
gopubmedrs797045289
geneviewrs797045289
scholarrs797045289
googlers797045289
pharmgkbrs797045289
gwascentralrs797045289
openSNPrs797045289
23andMers797045289
23andMe allrs797045289
SNP Nexus

SNPshotrs797045289
SNPdbers797045289
MSV3drs797045289
GWAS Ctlgrs797045289
Max Magnitude
ClinVar
Risk rs797045289(;)
Alt rs797045289(;)
Reference rs797045289(G;G)
Significance Pathogenic
Disease Lissencephaly 2
Variation info
Gene ARX
CLNDBN Lissencephaly 2, X-linked
Reversed 1
HGVS NC_000023.10:g.25028400delC
CLNSRC
CLNACC RCV000192868.1,