Have questions? Visit https://www.reddit.com/r/SNPedia

rs142073519

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs142073519(A;G)
Make rs142073519(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position5545246
GeneFARS2
is asnp
is mentioned by
dbSNPrs142073519
ebirs142073519
HLIrs142073519
Exacrs142073519
Varsomers142073519
Maprs142073519
PheGenIrs142073519
hapmaprs142073519
1000 genomesrs142073519
hgdprs142073519
ensemblrs142073519
gopubmedrs142073519
geneviewrs142073519
scholarrs142073519
googlers142073519
pharmgkbrs142073519
gwascentralrs142073519
openSNPrs142073519
23andMers142073519
23andMe allrs142073519
SNP Nexus

SNPshotrs142073519
SNPdbers142073519
MSV3drs142073519
GWAS Ctlgrs142073519
Max Magnitude0
ClinVar
Risk rs142073519(G;G)
Alt rs142073519(G;G)
Reference rs142073519(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FARS2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.5545479A>G
CLNSRC
CLNACC RCV000196488.2,