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rs1057517561

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517561(C;C)
Make rs1057517561(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position112827249
GeneAPC
is asnp
is mentioned by
dbSNPrs1057517561
dbSNP (classic)rs1057517561
ClinGenrs1057517561
ebirs1057517561
HLIrs1057517561
Exacrs1057517561
Gnomadrs1057517561
Varsomers1057517561
LitVarrs1057517561
Maprs1057517561
PheGenIrs1057517561
Biobankrs1057517561
1000 genomesrs1057517561
hgdprs1057517561
ensemblrs1057517561
geneviewrs1057517561
scholarrs1057517561
googlers1057517561
pharmgkbrs1057517561
gwascentralrs1057517561
openSNPrs1057517561
23andMers1057517561
SNPshotrs1057517561
SNPdbers1057517561
MSV3drs1057517561
GWAS Ctlgrs1057517561
Max Magnitude0
ClinVar
Risk rs1057517561(C;C)
Alt rs1057517561(C;C)
Reference Rs1057517561(T;T)
Significance Probable-Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112162946T>C
CLNSRC
CLNACC RCV000411158.1,