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rs1057520673

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520673(C;T)
Make rs1057520673(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position44860033
GeneEFTUD2
is asnp
is mentioned by
dbSNPrs1057520673
dbSNP (old)rs1057520673
ClinGenrs1057520673
ebirs1057520673
HLIrs1057520673
Exacrs1057520673
Gnomadrs1057520673
Varsomers1057520673
Maprs1057520673
PheGenIrs1057520673
Biobankrs1057520673
1000 genomesrs1057520673
hgdprs1057520673
ensemblrs1057520673
gopubmedrs1057520673
geneviewrs1057520673
scholarrs1057520673
googlers1057520673
pharmgkbrs1057520673
gwascentralrs1057520673
openSNPrs1057520673
23andMers1057520673
23andMe allrs1057520673
SNPshotrs1057520673
SNPdbers1057520673
MSV3drs1057520673
GWAS Ctlgrs1057520673
Max Magnitude0
ClinVar
Risk rs1057520673(T;T)
Alt rs1057520673(T;T)
Reference Rs1057520673(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene EFTUD2
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.42937401G>A
CLNSRC
CLNACC RCV000431548.1,