Rs104894741

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Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894741(A;A)
Make rs104894741(A;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position25012967
GeneARX
is asnp
is mentioned by
dbSNPrs104894741
PheGenIrs104894741
nextbiors104894741
hapmaprs104894741
1000 genomesrs104894741
hgdprs104894741
ensemblrs104894741
gopubmedrs104894741
geneviewrs104894741
scholarrs104894741
googlers104894741
pharmgkbrs104894741
gwascentralrs104894741
openSNPrs104894741
23andMers104894741
23andMe allrs104894741
SNP Nexus

SNPshotrs104894741
SNPdbers104894741
MSV3drs104894741
Merged fromRs28936076
Max Magnitude0
OMIM300382
Desc
Variant0012
Relatedalso
ClinVar
Risk rs104894741(A;A)
Alt rs104894741(A;A)
Reference rs104894741(T;T)
Significance Pathogenic
Disease X-linked lissencephaly 2
Variation info
Gene ARX
CLNDBN X-linked lissencephaly 2
Reversed 1
HGVS NC_000023.10:g.25031084A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011948.16,