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rs745595833

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs745595833(C;C)
Make rs745595833(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32753932
GeneYARS2
is asnp
is mentioned by
dbSNPrs745595833
ebirs745595833
HLIrs745595833
Exacrs745595833
Varsomers745595833
Maprs745595833
PheGenIrs745595833
hapmaprs745595833
1000 genomesrs745595833
hgdprs745595833
ensemblrs745595833
gopubmedrs745595833
geneviewrs745595833
scholarrs745595833
googlers745595833
pharmgkbrs745595833
gwascentralrs745595833
openSNPrs745595833
23andMers745595833
23andMe allrs745595833
SNP Nexus

SNPshotrs745595833
SNPdbers745595833
MSV3drs745595833
GWAS Ctlgrs745595833
Max Magnitude0
ClinVar
Risk rs745595833(A;A) rs745595833(C;C)
Alt rs745595833(A;A) rs745595833(C;C)
Reference Rs745595833(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene YARS2
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.32906866G>C
CLNSRC
CLNACC RCV000195520.2,