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rs863223958

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223958(C;G)
Make rs863223958(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position5368973
GeneFARS2
is asnp
is mentioned by
dbSNPrs863223958
ClinGenrs863223958
ebirs863223958
HLIrs863223958
Exacrs863223958
Varsomers863223958
Maprs863223958
PheGenIrs863223958
hapmaprs863223958
1000 genomesrs863223958
hgdprs863223958
ensemblrs863223958
gopubmedrs863223958
geneviewrs863223958
scholarrs863223958
googlers863223958
pharmgkbrs863223958
gwascentralrs863223958
openSNPrs863223958
23andMers863223958
23andMe allrs863223958
SNP Nexus

SNPshotrs863223958
SNPdbers863223958
MSV3drs863223958
GWAS Ctlgrs863223958
Max Magnitude0
ClinVar
Risk rs863223958(G;G)
Alt rs863223958(G;G)
Reference Rs863223958(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FARS2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.5369206C>G
CLNSRC
CLNACC RCV000197422.1,