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rs1064796941

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome17
Position56594563
GeneNOG
is asnp
is mentioned by
dbSNPrs1064796941
dbSNP (old)rs1064796941
ClinGenrs1064796941
ebirs1064796941
HLIrs1064796941
Exacrs1064796941
Gnomadrs1064796941
Varsomers1064796941
Maprs1064796941
PheGenIrs1064796941
Biobankrs1064796941
1000 genomesrs1064796941
hgdprs1064796941
ensemblrs1064796941
gopubmedrs1064796941
geneviewrs1064796941
scholarrs1064796941
googlers1064796941
pharmgkbrs1064796941
gwascentralrs1064796941
openSNPrs1064796941
23andMers1064796941
23andMe allrs1064796941
SNPshotrs1064796941
SNPdbers1064796941
MSV3drs1064796941
GWAS Ctlgrs1064796941
Max Magnitude0
ClinVar
Risk rs1064796941(A;A)
Alt rs1064796941(A;A)
Reference Rs1064796941(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NOG
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.54671924G>A
CLNSRC
CLNACC RCV000486797.1,