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rs1064796858

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome3
Position189974557
GeneP3H2
is asnp
is mentioned by
dbSNPrs1064796858
dbSNP (old)rs1064796858
ClinGenrs1064796858
ebirs1064796858
HLIrs1064796858
Exacrs1064796858
Gnomadrs1064796858
Varsomers1064796858
Maprs1064796858
PheGenIrs1064796858
Biobankrs1064796858
1000 genomesrs1064796858
hgdprs1064796858
ensemblrs1064796858
gopubmedrs1064796858
geneviewrs1064796858
scholarrs1064796858
googlers1064796858
pharmgkbrs1064796858
gwascentralrs1064796858
openSNPrs1064796858
23andMers1064796858
23andMe allrs1064796858
SNPshotrs1064796858
SNPdbers1064796858
MSV3drs1064796858
GWAS Ctlgrs1064796858
Max Magnitude0
ClinVar
Risk rs1064796858(T;T)
Alt rs1064796858(T;T)
Reference Rs1064796858(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene P3H2
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.189692346C>A
CLNSRC
CLNACC RCV000486475.1,