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rs137854568

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854568(C;T)
Make rs137854568(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position112815564
GeneAPC
is asnp
is mentioned by
dbSNPrs137854568
ebirs137854568
HLIrs137854568
Exacrs137854568
Varsomers137854568
Maprs137854568
PheGenIrs137854568
hapmaprs137854568
1000 genomesrs137854568
hgdprs137854568
ensemblrs137854568
gopubmedrs137854568
geneviewrs137854568
scholarrs137854568
googlers137854568
pharmgkbrs137854568
gwascentralrs137854568
openSNPrs137854568
23andMers137854568
23andMe allrs137854568
SNP Nexus

SNPshotrs137854568
SNPdbers137854568
MSV3drs137854568
GWAS Ctlgrs137854568
Max Magnitude0
OMIM611731
Desc
Variant0006
Relatedalso
ClinVar
Risk rs137854568(T;T)
Alt rs137854568(T;T)
Reference rs137854568(C;C)
Significance Pathogenic
Disease Familial adenomatous polyposis 1 Gardner syndrome not provided Hereditary cancer-predisposing syndrome Colorectal cancer
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1 Gardner syndrome not provided Hereditary cancer-predisposing syndrome Colorectal cancer, susceptibility to
Reversed 0
HGVS NC_000005.9:g.112151261C>T
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000000834.3, RCV000000835.4, RCV000077996.5, RCV000164370.1, RCV000210154.1,