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rs886039346

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs886039346(C;T)
Make rs886039346(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome20
Position63488423
GeneEEF1A2
is asnp
is mentioned by
dbSNPrs886039346
dbSNP (classic)rs886039346
ClinGenrs886039346
ebirs886039346
HLIrs886039346
Exacrs886039346
Gnomadrs886039346
Varsomers886039346
LitVarrs886039346
Maprs886039346
PheGenIrs886039346
Biobankrs886039346
1000 genomesrs886039346
hgdprs886039346
ensemblrs886039346
geneviewrs886039346
scholarrs886039346
googlers886039346
pharmgkbrs886039346
gwascentralrs886039346
openSNPrs886039346
23andMers886039346
SNPshotrs886039346
SNPdbers886039346
MSV3drs886039346
GWAS Ctlgrs886039346
Max Magnitude0
ClinVar
Risk rs886039346(T;T)
Alt rs886039346(T;T)
Reference Rs886039346(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene EEF1A2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62119776G>A
CLNSRC
CLNACC RCV000255580.1,