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rs863223957

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223957(A;A)
Make rs863223957(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position5545264
GeneFARS2
is asnp
is mentioned by
dbSNPrs863223957
ebirs863223957
HLIrs863223957
Exacrs863223957
Varsomers863223957
Maprs863223957
PheGenIrs863223957
hapmaprs863223957
1000 genomesrs863223957
hgdprs863223957
ensemblrs863223957
gopubmedrs863223957
geneviewrs863223957
scholarrs863223957
googlers863223957
pharmgkbrs863223957
gwascentralrs863223957
openSNPrs863223957
23andMers863223957
23andMe allrs863223957
SNP Nexus

SNPshotrs863223957
SNPdbers863223957
MSV3drs863223957
GWAS Ctlgrs863223957
Max Magnitude0
ClinVar
Risk rs863223957(A;A)
Alt rs863223957(A;A)
Reference rs863223957(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene FARS2
CLNDBN not specified
Reversed 0
HGVS NC_000006.11:g.5545497G>A
CLNSRC
CLNACC RCV000198248.1,