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rs1064796381

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome17
Position44854283
GeneEFTUD2
is asnp
is mentioned by
dbSNPrs1064796381
dbSNP (old)rs1064796381
ClinGenrs1064796381
ebirs1064796381
HLIrs1064796381
Exacrs1064796381
Gnomadrs1064796381
Varsomers1064796381
Maprs1064796381
PheGenIrs1064796381
Biobankrs1064796381
1000 genomesrs1064796381
hgdprs1064796381
ensemblrs1064796381
gopubmedrs1064796381
geneviewrs1064796381
scholarrs1064796381
googlers1064796381
pharmgkbrs1064796381
gwascentralrs1064796381
openSNPrs1064796381
23andMers1064796381
23andMe allrs1064796381
SNPshotrs1064796381
SNPdbers1064796381
MSV3drs1064796381
GWAS Ctlgrs1064796381
Max Magnitude0
ClinVar
Risk rs1064796381(A;A)
Alt rs1064796381(A;A)
Reference Rs1064796381(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EFTUD2
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.42931651G>T
CLNSRC
CLNACC RCV000480810.1,