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rs122453119

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs122453119(C;T)
Make rs122453119(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position133754153
GeneGPC3
is asnp
is mentioned by
dbSNPrs122453119
ebirs122453119
HLIrs122453119
Exacrs122453119
Varsomers122453119
Maprs122453119
PheGenIrs122453119
hapmaprs122453119
1000 genomesrs122453119
hgdprs122453119
ensemblrs122453119
gopubmedrs122453119
geneviewrs122453119
scholarrs122453119
googlers122453119
pharmgkbrs122453119
gwascentralrs122453119
openSNPrs122453119
23andMers122453119
23andMe allrs122453119
SNP Nexus

SNPshotrs122453119
SNPdbers122453119
MSV3drs122453119
GWAS Ctlgrs122453119
Max Magnitude0
OMIM300037
Desc
Variant0006
Relatedalso
ClinVar
Risk rs122453119(T;T)
Alt rs122453119(T;T)
Reference rs122453119(C;C)
Significance Pathogenic
Disease Wilms tumor 1
Variation info
Gene GPC3
CLNDBN Wilms tumor 1
Reversed 1
HGVS NC_000023.10:g.132888180G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012456.5,