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rs786201801

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786201801(C;T)
Make rs786201801(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112840215
GeneAPC
is asnp
is mentioned by
dbSNPrs786201801
ebirs786201801
HLIrs786201801
Exacrs786201801
Varsomers786201801
Maprs786201801
PheGenIrs786201801
hapmaprs786201801
1000 genomesrs786201801
hgdprs786201801
ensemblrs786201801
gopubmedrs786201801
geneviewrs786201801
scholarrs786201801
googlers786201801
pharmgkbrs786201801
gwascentralrs786201801
openSNPrs786201801
23andMers786201801
23andMe allrs786201801
SNP Nexus

SNPshotrs786201801
SNPdbers786201801
MSV3drs786201801
GWAS Ctlgrs786201801
Max Magnitude0
ClinVar
Risk rs786201801(T;T)
Alt rs786201801(T;T)
Reference rs786201801(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.112175912C>T
CLNSRC
CLNACC RCV000164276.1,