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rs1057521655

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521655(G;T)
Make rs1057521655(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position63488381
GeneEEF1A2
is asnp
is mentioned by
dbSNPrs1057521655
dbSNP (classic)rs1057521655
ClinGenrs1057521655
ebirs1057521655
HLIrs1057521655
Exacrs1057521655
Gnomadrs1057521655
Varsomers1057521655
LitVarrs1057521655
Maprs1057521655
PheGenIrs1057521655
Biobankrs1057521655
1000 genomesrs1057521655
hgdprs1057521655
ensemblrs1057521655
geneviewrs1057521655
scholarrs1057521655
googlers1057521655
pharmgkbrs1057521655
gwascentralrs1057521655
openSNPrs1057521655
23andMers1057521655
SNPshotrs1057521655
SNPdbers1057521655
MSV3drs1057521655
GWAS Ctlgrs1057521655
Max Magnitude0
ClinVar
Risk rs1057521655(T;T)
Alt rs1057521655(T;T)
Reference Rs1057521655(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EEF1A2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62119734C>A
CLNSRC
CLNACC RCV000441974.1,