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rs397514032

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397514032(-;-)
Make rs397514032(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112828924
GeneAPC
is asnp
is mentioned by
dbSNPrs397514032
ebirs397514032
HLIrs397514032
Exacrs397514032
Varsomers397514032
Maprs397514032
PheGenIrs397514032
hapmaprs397514032
1000 genomesrs397514032
hgdprs397514032
ensemblrs397514032
gopubmedrs397514032
geneviewrs397514032
scholarrs397514032
googlers397514032
pharmgkbrs397514032
gwascentralrs397514032
openSNPrs397514032
23andMers397514032
23andMe allrs397514032
SNP Nexus

SNPshotrs397514032
SNPdbers397514032
MSV3drs397514032
GWAS Ctlgrs397514032
Max Magnitude0
ClinVar
Risk rs397514032(;)
Alt rs397514032(;)
Reference rs397514032(A;A)
Significance Pathogenic
Disease Hepatocellular carcinoma
Variation info
Gene APC
CLNDBN Hepatocellular carcinoma
Reversed 0
HGVS NC_000005.9:g.112164621delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000000883.4,