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rs376213437

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs376213437(C;C)
Make rs376213437(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112767256
GeneAPC
is asnp
is mentioned by
dbSNPrs376213437
ebirs376213437
HLIrs376213437
Exacrs376213437
Varsomers376213437
Maprs376213437
PheGenIrs376213437
hapmaprs376213437
1000 genomesrs376213437
hgdprs376213437
ensemblrs376213437
gopubmedrs376213437
geneviewrs376213437
scholarrs376213437
googlers376213437
pharmgkbrs376213437
gwascentralrs376213437
openSNPrs376213437
23andMers376213437
23andMe allrs376213437
SNP Nexus

SNPshotrs376213437
SNPdbers376213437
MSV3drs376213437
GWAS Ctlgrs376213437
Max Magnitude0
ClinVar
Risk rs376213437(A,C,G;A,C,G)
Alt rs376213437(A,C,G;A,C,G)
Reference rs376213437(T;T)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN not provided Hereditary cancer-predisposing syndrome Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112102953T>A; NC_000005.9:g.112102953T>C; NC_000005.9:g.112102953T>G
CLNSRC
CLNACC RCV000159585.2, RCV000165334.1, RCV000205434.1, RCV000202141.1,