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rs757556226

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs757556226(A;A)
Make rs757556226(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position63488308
GeneEEF1A2
is asnp
is mentioned by
dbSNPrs757556226
dbSNP (classic)rs757556226
ClinGenrs757556226
ebirs757556226
HLIrs757556226
Exacrs757556226
Gnomadrs757556226
Varsomers757556226
LitVarrs757556226
Maprs757556226
PheGenIrs757556226
Biobankrs757556226
1000 genomesrs757556226
hgdprs757556226
ensemblrs757556226
geneviewrs757556226
scholarrs757556226
googlers757556226
pharmgkbrs757556226
gwascentralrs757556226
openSNPrs757556226
23andMers757556226
SNPshotrs757556226
SNPdbers757556226
MSV3drs757556226
GWAS Ctlgrs757556226
Max Magnitude0
ClinVar
Risk rs757556226(A;A)
Alt rs757556226(A;A)
Reference Rs757556226(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EEF1A2
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.62119661G>A
CLNSRC
CLNACC RCV000427894.1,