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rs137854573

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854573(C;T)
Make rs137854573(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position112828889
GeneAPC
is asnp
is mentioned by
dbSNPrs137854573
ebirs137854573
HLIrs137854573
Exacrs137854573
Varsomers137854573
Maprs137854573
PheGenIrs137854573
hapmaprs137854573
1000 genomesrs137854573
hgdprs137854573
ensemblrs137854573
gopubmedrs137854573
geneviewrs137854573
scholarrs137854573
googlers137854573
pharmgkbrs137854573
gwascentralrs137854573
openSNPrs137854573
23andMers137854573
23andMe allrs137854573
SNP Nexus

SNPshotrs137854573
SNPdbers137854573
MSV3drs137854573
GWAS Ctlgrs137854573
Max Magnitude0
OMIM611731
Desc
Variant0015
Relatedalso
ClinVar
Risk rs137854573(T;T)
Alt rs137854573(T;T)
Reference rs137854573(C;C)
Significance Pathogenic
Disease Familial adenomatous polyposis 1 Hereditary cancer-predisposing syndrome Colorectal cancer
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1 Hereditary cancer-predisposing syndrome Colorectal cancer, susceptibility to
Reversed 0
HGVS NC_000005.9:g.112164586C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000845.3, RCV000129303.1, RCV000210172.1,