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rs1060503318

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060503318(G;T)
Make rs1060503318(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position112835165
GeneAPC
is asnp
is mentioned by
dbSNPrs1060503318
dbSNP (classic)rs1060503318
ClinGenrs1060503318
ebirs1060503318
HLIrs1060503318
Exacrs1060503318
Gnomadrs1060503318
Varsomers1060503318
LitVarrs1060503318
Maprs1060503318
PheGenIrs1060503318
Biobankrs1060503318
1000 genomesrs1060503318
hgdprs1060503318
ensemblrs1060503318
geneviewrs1060503318
scholarrs1060503318
googlers1060503318
pharmgkbrs1060503318
gwascentralrs1060503318
openSNPrs1060503318
23andMers1060503318
23andMe allrs1060503318
SNPshotrs1060503318
SNPdbers1060503318
MSV3drs1060503318
GWAS Ctlgrs1060503318
Max Magnitude0
ClinVar
Risk rs1060503318(A;A) rs1060503318(T;T)
Alt rs1060503318(A;A) rs1060503318(T;T)
Reference Rs1060503318(G;G)
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.112170862G>A; NC_000005.9:g.112170862G>T
CLNSRC
CLNACC RCV000491686.1, RCV000462234.1, RCV000491095.1,