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rs113432057

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs113432057(C;T)
Make rs113432057(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome9
Position328076
GeneDOCK8
is asnp
is mentioned by
dbSNPrs113432057
dbSNP (old)rs113432057
ClinGenrs113432057
ebirs113432057
HLIrs113432057
Exacrs113432057
Gnomadrs113432057
Varsomers113432057
Maprs113432057
PheGenIrs113432057
Biobankrs113432057
1000 genomesrs113432057
hgdprs113432057
ensemblrs113432057
gopubmedrs113432057
geneviewrs113432057
scholarrs113432057
googlers113432057
pharmgkbrs113432057
gwascentralrs113432057
openSNPrs113432057
23andMers113432057
23andMe allrs113432057
SNPshotrs113432057
SNPdbers113432057
MSV3drs113432057
GWAS Ctlgrs113432057
Max Magnitude0
ClinVar
Risk rs113432057(T;T)
Alt rs113432057(T;T)
Reference Rs113432057(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DOCK8
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.328076C>T
CLNSRC
CLNACC RCV000398158.1,