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rs1064797069

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome17
Position44880594
GeneEFTUD2
is asnp
is mentioned by
dbSNPrs1064797069
dbSNP (old)rs1064797069
ClinGenrs1064797069
ebirs1064797069
HLIrs1064797069
Exacrs1064797069
Gnomadrs1064797069
Varsomers1064797069
Maprs1064797069
PheGenIrs1064797069
Biobankrs1064797069
1000 genomesrs1064797069
hgdprs1064797069
ensemblrs1064797069
gopubmedrs1064797069
geneviewrs1064797069
scholarrs1064797069
googlers1064797069
pharmgkbrs1064797069
gwascentralrs1064797069
openSNPrs1064797069
23andMers1064797069
23andMe allrs1064797069
SNPshotrs1064797069
SNPdbers1064797069
MSV3drs1064797069
GWAS Ctlgrs1064797069
Max Magnitude0
ClinVar
Risk rs1064797069(-;-)
Alt rs1064797069(-;-)
Reference Rs1064797069(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene EFTUD2
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.42957962delG
CLNSRC
CLNACC RCV000485356.1,