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rs554931092

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs554931092(A;A)
Make rs554931092(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position5369120
GeneFARS2
is asnp
is mentioned by
dbSNPrs554931092
ebirs554931092
HLIrs554931092
Exacrs554931092
Varsomers554931092
Maprs554931092
PheGenIrs554931092
hapmaprs554931092
1000 genomesrs554931092
hgdprs554931092
ensemblrs554931092
gopubmedrs554931092
geneviewrs554931092
scholarrs554931092
googlers554931092
pharmgkbrs554931092
gwascentralrs554931092
openSNPrs554931092
23andMers554931092
23andMe allrs554931092
SNP Nexus

SNPshotrs554931092
SNPdbers554931092
MSV3drs554931092
GWAS Ctlgrs554931092
Max Magnitude0
ClinVar
Risk rs554931092(A;A)
Alt rs554931092(A;A)
Reference rs554931092(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FARS2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.5369353G>A
CLNSRC
CLNACC RCV000199293.2,