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rs137854571

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854571(C;T)
Make rs137854571(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position112838793
GeneAPC
is asnp
is mentioned by
dbSNPrs137854571
ebirs137854571
HLIrs137854571
Exacrs137854571
Varsomers137854571
Maprs137854571
PheGenIrs137854571
hapmaprs137854571
1000 genomesrs137854571
hgdprs137854571
ensemblrs137854571
gopubmedrs137854571
geneviewrs137854571
scholarrs137854571
googlers137854571
pharmgkbrs137854571
gwascentralrs137854571
openSNPrs137854571
23andMers137854571
23andMe allrs137854571
SNP Nexus

SNPshotrs137854571
SNPdbers137854571
MSV3drs137854571
GWAS Ctlgrs137854571
Max Magnitude0
OMIM611731
Desc
Variant0011
Relatedalso
ClinVar
Risk rs137854571(T;T)
Alt rs137854571(T;T)
Reference rs137854571(C;C)
Significance Pathogenic
Disease Neoplasm of stomach
Variation info
Gene APC
CLNDBN Neoplasm of stomach
Reversed 0
HGVS NC_000005.9:g.112174490C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000840.4,