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rs863224271

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224271(G;T)
Make rs863224271(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position32755639
GeneYARS2
is asnp
is mentioned by
dbSNPrs863224271
ebirs863224271
HLIrs863224271
Exacrs863224271
Varsomers863224271
Maprs863224271
PheGenIrs863224271
hapmaprs863224271
1000 genomesrs863224271
hgdprs863224271
ensemblrs863224271
gopubmedrs863224271
geneviewrs863224271
scholarrs863224271
googlers863224271
pharmgkbrs863224271
gwascentralrs863224271
openSNPrs863224271
23andMers863224271
23andMe allrs863224271
SNP Nexus

SNPshotrs863224271
SNPdbers863224271
MSV3drs863224271
GWAS Ctlgrs863224271
Max Magnitude0
ClinVar
Risk rs863224271(T;T)
Alt rs863224271(T;T)
Reference rs863224271(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene YARS2
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.32908573C>A
CLNSRC
CLNACC RCV000199921.2,