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rs1060503336

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060503336(A;A)
Make rs1060503336(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position112837690
GeneAPC
is asnp
is mentioned by
dbSNPrs1060503336
dbSNP (old)rs1060503336
ClinGenrs1060503336
ebirs1060503336
HLIrs1060503336
Exacrs1060503336
Gnomadrs1060503336
Varsomers1060503336
Maprs1060503336
PheGenIrs1060503336
Biobankrs1060503336
1000 genomesrs1060503336
hgdprs1060503336
ensemblrs1060503336
gopubmedrs1060503336
geneviewrs1060503336
scholarrs1060503336
googlers1060503336
pharmgkbrs1060503336
gwascentralrs1060503336
openSNPrs1060503336
23andMers1060503336
23andMe allrs1060503336
SNPshotrs1060503336
SNPdbers1060503336
MSV3drs1060503336
GWAS Ctlgrs1060503336
Max Magnitude0
ClinVar
Risk rs1060503336(A;A)
Alt rs1060503336(A;A)
Reference Rs1060503336(G;G)
Significance 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.112173387G>A
CLNSRC
CLNACC RCV000472625.1, RCV000491133.1,