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rs137854569

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854569(C;G)
Make rs137854569(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position112815499
GeneAPC
is asnp
is mentioned by
dbSNPrs137854569
ebirs137854569
HLIrs137854569
Exacrs137854569
Varsomers137854569
Maprs137854569
PheGenIrs137854569
hapmaprs137854569
1000 genomesrs137854569
hgdprs137854569
ensemblrs137854569
gopubmedrs137854569
geneviewrs137854569
scholarrs137854569
googlers137854569
pharmgkbrs137854569
gwascentralrs137854569
openSNPrs137854569
23andMers137854569
23andMe allrs137854569
SNP Nexus

SNPshotrs137854569
SNPdbers137854569
MSV3drs137854569
GWAS Ctlgrs137854569
Max Magnitude0
OMIM611731
Desc
Variant0007
Relatedalso
ClinVar
Risk rs137854569(G,T;G,T)
Alt rs137854569(G,T;G,T)
Reference rs137854569(C;C)
Significance Pathogenic
Disease Gardner syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene APC
CLNDBN Gardner syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000005.9:g.112151196C>G; NC_000005.9:g.112151196C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000836.4, RCV000218327.1,