Rs104894743

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Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894743(C;T)
Make rs104894743(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position25012937
GeneARX
is asnp
is mentioned by
dbSNPrs104894743
Exacrs104894743
PheGenIrs104894743
nextbiors104894743
hapmaprs104894743
1000 genomesrs104894743
hgdprs104894743
ensemblrs104894743
gopubmedrs104894743
geneviewrs104894743
scholarrs104894743
googlers104894743
pharmgkbrs104894743
gwascentralrs104894743
openSNPrs104894743
23andMers104894743
23andMe allrs104894743
SNP Nexus

SNPshotrs104894743
SNPdbers104894743
MSV3drs104894743
Merged fromRs28936074
OMIM300382
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104894743(T;T)
Alt rs104894743(T;T)
Reference rs104894743(C;C)
Significance Pathogenic
Disease West syndrome
Variation info
Gene ARX
CLNDBN West syndrome
Reversed 1
HGVS NC_000023.10:g.25031054G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011939.4,