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rs137854578

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137854578(A;T)
Make rs137854578(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position112839777
GeneAPC
is asnp
is mentioned by
dbSNPrs137854578
ebirs137854578
HLIrs137854578
Exacrs137854578
Varsomers137854578
Maprs137854578
PheGenIrs137854578
hapmaprs137854578
1000 genomesrs137854578
hgdprs137854578
ensemblrs137854578
gopubmedrs137854578
geneviewrs137854578
scholarrs137854578
googlers137854578
pharmgkbrs137854578
gwascentralrs137854578
openSNPrs137854578
23andMers137854578
23andMe allrs137854578
SNP Nexus

SNPshotrs137854578
SNPdbers137854578
MSV3drs137854578
GWAS Ctlgrs137854578
Max Magnitude0
OMIM611731
Desc
Variant0024
Relatedalso
ClinVar
Risk rs137854578(T;T)
Alt rs137854578(T;T)
Reference rs137854578(A;A)
Significance Pathogenic
Disease Hepatoblastoma
Variation info
Gene APC
CLNDBN Hepatoblastoma
Reversed 0
HGVS NC_000005.9:g.112175474A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000859.4,