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rs137854577

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854577(C;T)
Make rs137854577(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position112780901
GeneAPC
is asnp
is mentioned by
dbSNPrs137854577
ebirs137854577
HLIrs137854577
Exacrs137854577
Varsomers137854577
Maprs137854577
PheGenIrs137854577
hapmaprs137854577
1000 genomesrs137854577
hgdprs137854577
ensemblrs137854577
gopubmedrs137854577
geneviewrs137854577
scholarrs137854577
googlers137854577
pharmgkbrs137854577
gwascentralrs137854577
openSNPrs137854577
23andMers137854577
23andMe allrs137854577
SNP Nexus

SNPshotrs137854577
SNPdbers137854577
MSV3drs137854577
GWAS Ctlgrs137854577
Max Magnitude0
OMIM611731
Desc
Variant0022
Relatedalso
ClinVar
Risk rs137854577(T;T)
Alt rs137854577(T;T)
Reference rs137854577(C;C)
Significance Pathogenic
Disease Familial adenomatous polyposis 1 Brain tumor-polyposis syndrome 2 not provided
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1 Brain tumor-polyposis syndrome 2 not provided
Reversed 0
HGVS NC_000005.9:g.112116598C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000853.1, RCV000000854.1, RCV000202265.2,