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rs137854576

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854576(A;A)
Make rs137854576(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position112775676
GeneAPC
is asnp
is mentioned by
dbSNPrs137854576
ebirs137854576
HLIrs137854576
Exacrs137854576
Varsomers137854576
Maprs137854576
PheGenIrs137854576
hapmaprs137854576
1000 genomesrs137854576
hgdprs137854576
ensemblrs137854576
gopubmedrs137854576
geneviewrs137854576
scholarrs137854576
googlers137854576
pharmgkbrs137854576
gwascentralrs137854576
openSNPrs137854576
23andMers137854576
23andMe allrs137854576
SNP Nexus

SNPshotrs137854576
SNPdbers137854576
MSV3drs137854576
GWAS Ctlgrs137854576
Max Magnitude0
OMIM611731
Desc
Variant0021
Relatedalso
ClinVar
Risk rs137854576(A;A)
Alt rs137854576(A;A)
Reference rs137854576(G;G)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112111373G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000852.2,