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rs1064796986

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome4
Position39205167
GeneWDR19
is asnp
is mentioned by
dbSNPrs1064796986
dbSNP (old)rs1064796986
ClinGenrs1064796986
ebirs1064796986
HLIrs1064796986
Exacrs1064796986
Gnomadrs1064796986
Varsomers1064796986
Maprs1064796986
PheGenIrs1064796986
Biobankrs1064796986
1000 genomesrs1064796986
hgdprs1064796986
ensemblrs1064796986
gopubmedrs1064796986
geneviewrs1064796986
scholarrs1064796986
googlers1064796986
pharmgkbrs1064796986
gwascentralrs1064796986
openSNPrs1064796986
23andMers1064796986
23andMe allrs1064796986
SNPshotrs1064796986
SNPdbers1064796986
MSV3drs1064796986
GWAS Ctlgrs1064796986
Max Magnitude0
ClinVar
Risk rs1064796986(C;C)
Alt rs1064796986(C;C)
Reference Rs1064796986(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene WDR19
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.39206787T>C
CLNSRC
CLNACC RCV000479045.1,