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rs137854580

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854580(C;T)
Make rs137854580(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position112827194
GeneAPC
is asnp
is mentioned by
dbSNPrs137854580
ebirs137854580
HLIrs137854580
Exacrs137854580
Varsomers137854580
Maprs137854580
PheGenIrs137854580
hapmaprs137854580
1000 genomesrs137854580
hgdprs137854580
ensemblrs137854580
gopubmedrs137854580
geneviewrs137854580
scholarrs137854580
googlers137854580
pharmgkbrs137854580
gwascentralrs137854580
openSNPrs137854580
23andMers137854580
23andMe allrs137854580
SNP Nexus

SNPshotrs137854580
SNPdbers137854580
MSV3drs137854580
GWAS Ctlgrs137854580
Max Magnitude0
OMIM611731
Desc
Variant0031
Relatedalso
ClinVar
Risk rs137854580(G,T;G,T)
Alt rs137854580(G,T;G,T)
Reference rs137854580(C;C)
Significance Pathogenic
Disease not provided Gardner syndrome Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN not provided Gardner syndrome Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112162891C>G; NC_000005.9:g.112162891C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000034403.1, RCV000000867.2, RCV000204796.2,