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rs137854574

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854574(C;T)
Make rs137854574(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position112828919
GeneAPC
is asnp
is mentioned by
dbSNPrs137854574
ebirs137854574
HLIrs137854574
Exacrs137854574
Varsomers137854574
Maprs137854574
PheGenIrs137854574
hapmaprs137854574
1000 genomesrs137854574
hgdprs137854574
ensemblrs137854574
gopubmedrs137854574
geneviewrs137854574
scholarrs137854574
googlers137854574
pharmgkbrs137854574
gwascentralrs137854574
openSNPrs137854574
23andMers137854574
23andMe allrs137854574
SNP Nexus

SNPshotrs137854574
SNPdbers137854574
MSV3drs137854574
GWAS Ctlgrs137854574
Max Magnitude0
OMIM611731
Desc
Variant0016
Relatedalso
ClinVar
Risk rs137854574(T;T)
Alt rs137854574(T;T)
Reference rs137854574(C;C)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112164616C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000846.3,