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rs351771

From SNPedia

Orientationminus
Stabilizedplus
Make rs351771(C;C)
Make rs351771(C;T)
Make rs351771(T;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position112828864
GeneAPC
is asnp
is mentioned by
dbSNPrs351771
ebirs351771
HLIrs351771
Exacrs351771
Varsomers351771
Maprs351771
PheGenIrs351771
hapmaprs351771
1000 genomesrs351771
hgdprs351771
ensemblrs351771
gopubmedrs351771
geneviewrs351771
scholarrs351771
googlers351771
pharmgkbrs351771
gwascentralrs351771
openSNPrs351771
23andMers351771
23andMe allrs351771
SNP Nexus

SNPshotrs351771
SNPdbers351771
MSV3drs351771
GWAS Ctlgrs351771
GMAF0.3393
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 24078348OA-icon.png] An Analysis of Polymorphisms Within the Wnt Signaling Pathway in Relation to Ovarian Cancer Risk in a Polish Population


[PMID 16569251OA-icon.png] Single nucleotide polymorphisms of the APC gene and colorectal cancer risk: a case-control study in Taiwan.


[PMID 18849522OA-icon.png] Nested Patch PCR enables highly multiplexed mutation discovery in candidate genes.


[PMID 20333795OA-icon.png] APC gene mutations in Chinese familial adenomatous polyposis patients.


ClinVar
Risk rs351771(T;T)
Alt rs351771(T;T)
Reference rs351771(C;C)
Significance Other
Disease not specified Familial colorectal cancer Hereditary cancer-predisposing syndrome
Variation info
Gene APC
CLNDBN not specified Familial colorectal cancer Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000005.9:g.112164561G>A
CLNSRC ClinVar Emory University
CLNACC RCV000035066.7, RCV000074153.1, RCV000162371.1,