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rs1057522002

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057522002(A;A)
Make rs1057522002(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position44883653
GeneEFTUD2
is asnp
is mentioned by
dbSNPrs1057522002
dbSNP (classic)rs1057522002
ClinGenrs1057522002
ebirs1057522002
HLIrs1057522002
Exacrs1057522002
Gnomadrs1057522002
Varsomers1057522002
LitVarrs1057522002
Maprs1057522002
PheGenIrs1057522002
Biobankrs1057522002
1000 genomesrs1057522002
hgdprs1057522002
ensemblrs1057522002
geneviewrs1057522002
scholarrs1057522002
googlers1057522002
pharmgkbrs1057522002
gwascentralrs1057522002
openSNPrs1057522002
23andMers1057522002
23andMe allrs1057522002
SNPshotrs1057522002
SNPdbers1057522002
MSV3drs1057522002
GWAS Ctlgrs1057522002
Max Magnitude0
ClinVar
Risk rs1057522002(A;A)
Alt rs1057522002(A;A)
Reference Rs1057522002(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EFTUD2
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.42961021C>T
CLNSRC
CLNACC RCV000428632.1,