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rs555093151

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs555093151(C;C)
Make rs555093151(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position32755694
GeneYARS2
is asnp
is mentioned by
dbSNPrs555093151
dbSNP (classic)rs555093151
ClinGenrs555093151
ebirs555093151
HLIrs555093151
Exacrs555093151
Gnomadrs555093151
Varsomers555093151
LitVarrs555093151
Maprs555093151
PheGenIrs555093151
Biobankrs555093151
1000 genomesrs555093151
hgdprs555093151
ensemblrs555093151
geneviewrs555093151
scholarrs555093151
googlers555093151
pharmgkbrs555093151
gwascentralrs555093151
openSNPrs555093151
23andMers555093151
SNPshotrs555093151
SNPdbers555093151
MSV3drs555093151
GWAS Ctlgrs555093151
Max Magnitude0
ClinVar
Risk rs555093151(A;A) rs555093151(C;C)
Alt rs555093151(A;A) rs555093151(C;C)
Reference Rs555093151(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene YARS2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.32908628G>C
CLNSRC
CLNACC RCV000433553.1,