Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057520674

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520674(G;T)
Make rs1057520674(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position44894419
GeneEFTUD2
is asnp
is mentioned by
dbSNPrs1057520674
dbSNP (classic)rs1057520674
ClinGenrs1057520674
ebirs1057520674
HLIrs1057520674
Exacrs1057520674
Gnomadrs1057520674
Varsomers1057520674
LitVarrs1057520674
Maprs1057520674
PheGenIrs1057520674
Biobankrs1057520674
1000 genomesrs1057520674
hgdprs1057520674
ensemblrs1057520674
geneviewrs1057520674
scholarrs1057520674
googlers1057520674
pharmgkbrs1057520674
gwascentralrs1057520674
openSNPrs1057520674
23andMers1057520674
23andMe allrs1057520674
SNPshotrs1057520674
SNPdbers1057520674
MSV3drs1057520674
GWAS Ctlgrs1057520674
Max Magnitude0
ClinVar
Risk rs1057520674(T;T)
Alt rs1057520674(T;T)
Reference Rs1057520674(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene EFTUD2
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.42971787C>A
CLNSRC
CLNACC RCV000427380.1,