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rs137854583

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854583(C;T)
Make rs137854583(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position112780880
GeneAPC
is asnp
is mentioned by
dbSNPrs137854583
ebirs137854583
HLIrs137854583
Exacrs137854583
Varsomers137854583
Maprs137854583
PheGenIrs137854583
hapmaprs137854583
1000 genomesrs137854583
hgdprs137854583
ensemblrs137854583
gopubmedrs137854583
geneviewrs137854583
scholarrs137854583
googlers137854583
pharmgkbrs137854583
gwascentralrs137854583
openSNPrs137854583
23andMers137854583
23andMe allrs137854583
SNP Nexus

SNPshotrs137854583
SNPdbers137854583
MSV3drs137854583
GWAS Ctlgrs137854583
Max Magnitude0
OMIM611731
Desc
Variant0047
Relatedalso
ClinVar
Risk rs137854583(A,T;A,T)
Alt rs137854583(A,T;A,T)
Reference rs137854583(C;C)
Significance Pathogenic
Disease Familial adenomatous polyposis 1 Gardner syndrome
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1 Gardner syndrome
Reversed 0
HGVS NC_000005.9:g.112116577C>A; NC_000005.9:g.112116577C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000144572.1, RCV000000882.2,