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rs1060503355

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060503355(C;T)
Make rs1060503355(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position112842570
GeneAPC
is asnp
is mentioned by
dbSNPrs1060503355
dbSNP (classic)rs1060503355
ClinGenrs1060503355
ebirs1060503355
HLIrs1060503355
Exacrs1060503355
Gnomadrs1060503355
Varsomers1060503355
LitVarrs1060503355
Maprs1060503355
PheGenIrs1060503355
Biobankrs1060503355
1000 genomesrs1060503355
hgdprs1060503355
ensemblrs1060503355
geneviewrs1060503355
scholarrs1060503355
googlers1060503355
pharmgkbrs1060503355
gwascentralrs1060503355
openSNPrs1060503355
23andMers1060503355
SNPshotrs1060503355
SNPdbers1060503355
MSV3drs1060503355
GWAS Ctlgrs1060503355
Max Magnitude0
ClinVar
Risk rs1060503355(T;T)
Alt rs1060503355(T;T)
Reference Rs1060503355(C;C)
Significance Probable-Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112178267C>T
CLNSRC
CLNACC RCV000460599.1,