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rs863224270

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224270(A;G)
Make rs863224270(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32747242
GeneYARS2
is asnp
is mentioned by
dbSNPrs863224270
ebirs863224270
HLIrs863224270
Exacrs863224270
Varsomers863224270
Maprs863224270
PheGenIrs863224270
hapmaprs863224270
1000 genomesrs863224270
hgdprs863224270
ensemblrs863224270
gopubmedrs863224270
geneviewrs863224270
scholarrs863224270
googlers863224270
pharmgkbrs863224270
gwascentralrs863224270
openSNPrs863224270
23andMers863224270
23andMe allrs863224270
SNP Nexus

SNPshotrs863224270
SNPdbers863224270
MSV3drs863224270
GWAS Ctlgrs863224270
Max Magnitude0
ClinVar
Risk rs863224270(G;G)
Alt rs863224270(G;G)
Reference rs863224270(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene YARS2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.32900176T>C
CLNSRC
CLNACC RCV000199469.1,