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rs786201856

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786201856(C;T)
Make rs786201856(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112815507
GeneAPC
is asnp
is mentioned by
dbSNPrs786201856
ebirs786201856
HLIrs786201856
Exacrs786201856
Varsomers786201856
Maprs786201856
PheGenIrs786201856
hapmaprs786201856
1000 genomesrs786201856
hgdprs786201856
ensemblrs786201856
gopubmedrs786201856
geneviewrs786201856
scholarrs786201856
googlers786201856
pharmgkbrs786201856
gwascentralrs786201856
openSNPrs786201856
23andMers786201856
23andMe allrs786201856
SNP Nexus

SNPshotrs786201856
SNPdbers786201856
MSV3drs786201856
GWAS Ctlgrs786201856
Max Magnitude0
ClinVar
Risk rs786201856(T;T)
Alt rs786201856(T;T)
Reference rs786201856(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome not provided Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112151204C>T
CLNSRC
CLNACC RCV000164351.1, RCV000202113.1, RCV000226000.1,