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rs1057517568

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517568(A;A)
Make rs1057517568(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position112841965
GeneAPC
is asnp
is mentioned by
dbSNPrs1057517568
dbSNP (old)rs1057517568
ClinGenrs1057517568
ebirs1057517568
HLIrs1057517568
Exacrs1057517568
Gnomadrs1057517568
Varsomers1057517568
Maprs1057517568
PheGenIrs1057517568
Biobankrs1057517568
1000 genomesrs1057517568
hgdprs1057517568
ensemblrs1057517568
gopubmedrs1057517568
geneviewrs1057517568
scholarrs1057517568
googlers1057517568
pharmgkbrs1057517568
gwascentralrs1057517568
openSNPrs1057517568
23andMers1057517568
23andMe allrs1057517568
SNPshotrs1057517568
SNPdbers1057517568
MSV3drs1057517568
GWAS Ctlgrs1057517568
Max Magnitude0
ClinVar
Risk rs1057517568(A;A)
Alt rs1057517568(A;A)
Reference Rs1057517568(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.112177662T>A
CLNSRC
CLNACC RCV000409307.1,