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rs202060864

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs202060864(C;T)
Make rs202060864(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position5404596
GeneFARS2
is asnp
is mentioned by
dbSNPrs202060864
ebirs202060864
HLIrs202060864
Exacrs202060864
Varsomers202060864
Maprs202060864
PheGenIrs202060864
hapmaprs202060864
1000 genomesrs202060864
hgdprs202060864
ensemblrs202060864
gopubmedrs202060864
geneviewrs202060864
scholarrs202060864
googlers202060864
pharmgkbrs202060864
gwascentralrs202060864
openSNPrs202060864
23andMers202060864
23andMe allrs202060864
SNP Nexus

SNPshotrs202060864
SNPdbers202060864
MSV3drs202060864
GWAS Ctlgrs202060864
Max Magnitude0
ClinVar
Risk rs202060864(T;T)
Alt rs202060864(T;T)
Reference rs202060864(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FARS2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.5404829C>T
CLNSRC
CLNACC RCV000196357.2,