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rs137854582

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137854582(A;A)
Make rs137854582(A;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position112837687
GeneAPC
is asnp
is mentioned by
dbSNPrs137854582
ebirs137854582
HLIrs137854582
Exacrs137854582
Varsomers137854582
Maprs137854582
PheGenIrs137854582
hapmaprs137854582
1000 genomesrs137854582
hgdprs137854582
ensemblrs137854582
gopubmedrs137854582
geneviewrs137854582
scholarrs137854582
googlers137854582
pharmgkbrs137854582
gwascentralrs137854582
openSNPrs137854582
23andMers137854582
23andMe allrs137854582
SNP Nexus

SNPshotrs137854582
SNPdbers137854582
MSV3drs137854582
GWAS Ctlgrs137854582
Max Magnitude0
OMIM611731
Desc
Variant0039
Relatedalso
ClinVar
Risk rs137854582(A;A)
Alt rs137854582(A;A)
Reference rs137854582(T;T)
Significance Pathogenic
Disease Gardner syndrome
Variation info
Gene APC
CLNDBN Gardner syndrome
Reversed 0
HGVS NC_000005.9:g.112173384T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000875.2,