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rs192864327

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs192864327(G;T)
Make rs192864327(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome9
Position271626
GeneDOCK8
is asnp
is mentioned by
dbSNPrs192864327
dbSNP (old)rs192864327
ClinGenrs192864327
ebirs192864327
HLIrs192864327
Exacrs192864327
Gnomadrs192864327
Varsomers192864327
Maprs192864327
PheGenIrs192864327
Biobankrs192864327
1000 genomesrs192864327
hgdprs192864327
ensemblrs192864327
gopubmedrs192864327
geneviewrs192864327
scholarrs192864327
googlers192864327
pharmgkbrs192864327
gwascentralrs192864327
openSNPrs192864327
23andMers192864327
23andMe allrs192864327
SNPshotrs192864327
SNPdbers192864327
MSV3drs192864327
GWAS Ctlgrs192864327
Max Magnitude0
ClinVar
Risk rs192864327(T;T)
Alt rs192864327(T;T)
Reference Rs192864327(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DOCK8
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.271626G>T
CLNSRC
CLNACC RCV000256030.2,