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rs1060503261

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060503261(A;A)
Make rs1060503261(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position112801383
GeneAPC
is asnp
is mentioned by
dbSNPrs1060503261
dbSNP (old)rs1060503261
ClinGenrs1060503261
ebirs1060503261
HLIrs1060503261
Exacrs1060503261
Gnomadrs1060503261
Varsomers1060503261
Maprs1060503261
PheGenIrs1060503261
Biobankrs1060503261
1000 genomesrs1060503261
hgdprs1060503261
ensemblrs1060503261
gopubmedrs1060503261
geneviewrs1060503261
scholarrs1060503261
googlers1060503261
pharmgkbrs1060503261
gwascentralrs1060503261
openSNPrs1060503261
23andMers1060503261
23andMe allrs1060503261
SNPshotrs1060503261
SNPdbers1060503261
MSV3drs1060503261
GWAS Ctlgrs1060503261
Max Magnitude0
ClinVar
Risk rs1060503261(A;A)
Alt rs1060503261(A;A)
Reference Rs1060503261(G;G)
Significance Probable-Pathogenic
Disease Familial adenomatous polyposis 1 Hereditary cancer-predisposing syndrome
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.112137080G>A
CLNSRC
CLNACC RCV000461938.1, RCV000491926.1,