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rs1060503333

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060503333(C;G)
Make rs1060503333(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position112821953
GeneAPC
is asnp
is mentioned by
dbSNPrs1060503333
dbSNP (old)rs1060503333
ClinGenrs1060503333
ebirs1060503333
HLIrs1060503333
Exacrs1060503333
Gnomadrs1060503333
Varsomers1060503333
LitVarrs1060503333
Maprs1060503333
PheGenIrs1060503333
Biobankrs1060503333
1000 genomesrs1060503333
hgdprs1060503333
ensemblrs1060503333
gopubmedrs1060503333
geneviewrs1060503333
scholarrs1060503333
googlers1060503333
pharmgkbrs1060503333
gwascentralrs1060503333
openSNPrs1060503333
23andMers1060503333
23andMe allrs1060503333
SNPshotrs1060503333
SNPdbers1060503333
MSV3drs1060503333
GWAS Ctlgrs1060503333
Max Magnitude0
ClinVar
Risk rs1060503333(G;G)
Alt rs1060503333(G;G)
Reference Rs1060503333(C;C)
Significance Pathogenic
Disease Familial adenomatous polyposis 1 not provided Hereditary cancer-predisposing syndrome
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1 not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.112157650C>G
CLNSRC
CLNACC RCV000470894.1, RCV000481642.1, RCV000491762.1,