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rs786204170

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204170(A;A)
Make rs786204170(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112839769
GeneAPC
is asnp
is mentioned by
dbSNPrs786204170
ebirs786204170
HLIrs786204170
Exacrs786204170
Varsomers786204170
Maprs786204170
PheGenIrs786204170
hapmaprs786204170
1000 genomesrs786204170
hgdprs786204170
ensemblrs786204170
gopubmedrs786204170
geneviewrs786204170
scholarrs786204170
googlers786204170
pharmgkbrs786204170
gwascentralrs786204170
openSNPrs786204170
23andMers786204170
23andMe allrs786204170
SNP Nexus

SNPshotrs786204170
SNPdbers786204170
MSV3drs786204170
GWAS Ctlgrs786204170
Max Magnitude0
ClinVar
Risk rs786204170(A;A)
Alt rs786204170(A;A)
Reference rs786204170(C;C)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112175466C>A
CLNSRC
CLNACC RCV000168194.1,