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rs863224272

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224272(C;C)
Make rs863224272(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32755501
GeneYARS2
is asnp
is mentioned by
dbSNPrs863224272
ClinGenrs863224272
ebirs863224272
HLIrs863224272
Exacrs863224272
Varsomers863224272
Maprs863224272
PheGenIrs863224272
hapmaprs863224272
1000 genomesrs863224272
hgdprs863224272
ensemblrs863224272
gopubmedrs863224272
geneviewrs863224272
scholarrs863224272
googlers863224272
pharmgkbrs863224272
gwascentralrs863224272
openSNPrs863224272
23andMers863224272
23andMe allrs863224272
SNP Nexus

SNPshotrs863224272
SNPdbers863224272
MSV3drs863224272
GWAS Ctlgrs863224272
Max Magnitude0
ClinVar
Risk rs863224272(C;C)
Alt rs863224272(C;C)
Reference Rs863224272(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene YARS2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.32908435C>G
CLNSRC
CLNACC RCV000196700.1,