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rs751459058

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs751459058(C;T)
Make rs751459058(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position5613185
GeneFARS2
is asnp
is mentioned by
dbSNPrs751459058
ebirs751459058
HLIrs751459058
Exacrs751459058
Varsomers751459058
Maprs751459058
PheGenIrs751459058
hapmaprs751459058
1000 genomesrs751459058
hgdprs751459058
ensemblrs751459058
gopubmedrs751459058
geneviewrs751459058
scholarrs751459058
googlers751459058
pharmgkbrs751459058
gwascentralrs751459058
openSNPrs751459058
23andMers751459058
23andMe allrs751459058
SNP Nexus

SNPshotrs751459058
SNPdbers751459058
MSV3drs751459058
GWAS Ctlgrs751459058
Max Magnitude0
ClinVar
Risk rs751459058(T;T)
Alt rs751459058(T;T)
Reference rs751459058(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FARS2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.5613418C>T
CLNSRC
CLNACC RCV000200808.2,