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rs786204169

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204169(G;G)
Make rs786204169(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112839424
GeneAPC
is asnp
is mentioned by
dbSNPrs786204169
ebirs786204169
HLIrs786204169
Exacrs786204169
Varsomers786204169
Maprs786204169
PheGenIrs786204169
hapmaprs786204169
1000 genomesrs786204169
hgdprs786204169
ensemblrs786204169
gopubmedrs786204169
geneviewrs786204169
scholarrs786204169
googlers786204169
pharmgkbrs786204169
gwascentralrs786204169
openSNPrs786204169
23andMers786204169
23andMe allrs786204169
SNP Nexus

SNPshotrs786204169
SNPdbers786204169
MSV3drs786204169
GWAS Ctlgrs786204169
Max Magnitude0
ClinVar
Risk rs786204169(G;G)
Alt rs786204169(G;G)
Reference rs786204169(T;T)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112175121T>G
CLNSRC
CLNACC RCV000168191.2,