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rs786201291

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786201291(A;G)
Make rs786201291(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112767187
GeneAPC
is asnp
is mentioned by
dbSNPrs786201291
ebirs786201291
HLIrs786201291
Exacrs786201291
Varsomers786201291
Maprs786201291
PheGenIrs786201291
hapmaprs786201291
1000 genomesrs786201291
hgdprs786201291
ensemblrs786201291
gopubmedrs786201291
geneviewrs786201291
scholarrs786201291
googlers786201291
pharmgkbrs786201291
gwascentralrs786201291
openSNPrs786201291
23andMers786201291
23andMe allrs786201291
SNP Nexus

SNPshotrs786201291
SNPdbers786201291
MSV3drs786201291
GWAS Ctlgrs786201291
Max Magnitude0
ClinVar
Risk rs786201291(G;G)
Alt rs786201291(G;G)
Reference rs786201291(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.112102884A>G
CLNSRC
CLNACC RCV000163246.1,