Have questions? Visit https://www.reddit.com/r/SNPedia

rs145945630

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs145945630(C;T)
Make rs145945630(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112754960
GeneAPC
is asnp
is mentioned by
dbSNPrs145945630
ebirs145945630
HLIrs145945630
Exacrs145945630
Varsomers145945630
Maprs145945630
PheGenIrs145945630
hapmaprs145945630
1000 genomesrs145945630
hgdprs145945630
ensemblrs145945630
gopubmedrs145945630
geneviewrs145945630
scholarrs145945630
googlers145945630
pharmgkbrs145945630
gwascentralrs145945630
openSNPrs145945630
23andMers145945630
23andMe allrs145945630
SNP Nexus

SNPshotrs145945630
SNPdbers145945630
MSV3drs145945630
GWAS Ctlgrs145945630
Max Magnitude0
ClinVar
Risk rs145945630(T;T)
Alt rs145945630(T;T)
Reference rs145945630(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112090657C>T
CLNSRC
CLNACC RCV000164002.1, RCV000227124.1,