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rs137854575

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854575(C;T)
Make rs137854575(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position112838399
GeneAPC
is asnp
is mentioned by
dbSNPrs137854575
ebirs137854575
HLIrs137854575
Exacrs137854575
Varsomers137854575
Maprs137854575
PheGenIrs137854575
hapmaprs137854575
1000 genomesrs137854575
hgdprs137854575
ensemblrs137854575
gopubmedrs137854575
geneviewrs137854575
scholarrs137854575
googlers137854575
pharmgkbrs137854575
gwascentralrs137854575
openSNPrs137854575
23andMers137854575
23andMe allrs137854575
SNP Nexus

SNPshotrs137854575
SNPdbers137854575
MSV3drs137854575
GWAS Ctlgrs137854575
GMAF0.0004591
Max Magnitude0
OMIM611731
Desc
Variant0018
Relatedalso
ClinVar
Risk rs137854575(A,G,T;A,G,T)
Alt rs137854575(A,G,T;A,G,T)
Reference rs137854575(C;C)
Significance Pathogenic
Disease Familial adenomatous polyposis 1 Hereditary cancer-predisposing syndrome not provided Colorectal cancer Familial multiple polyposis syndrome not specified
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1 Hereditary cancer-predisposing syndrome not provided Colorectal cancer, susceptibility to Familial multiple polyposis syndrome not specified
Reversed 0
HGVS NC_000005.9:g.112174096C>A; NC_000005.9:g.112174096C>G; NC_000005.9:g.112174096C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000848.3, RCV000129305.4, RCV000202012.1, RCV000210151.1, RCV000165582.1, RCV000202153.1, RCV000123663.5, RCV000199328.3, RCV000202773.1, RCV000211904.1,