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rs372054960

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs372054960(C;T)
Make rs372054960(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position5771293
GeneFARS2
is asnp
is mentioned by
dbSNPrs372054960
ebirs372054960
HLIrs372054960
Exacrs372054960
Varsomers372054960
Maprs372054960
PheGenIrs372054960
hapmaprs372054960
1000 genomesrs372054960
hgdprs372054960
ensemblrs372054960
gopubmedrs372054960
geneviewrs372054960
scholarrs372054960
googlers372054960
pharmgkbrs372054960
gwascentralrs372054960
openSNPrs372054960
23andMers372054960
23andMe allrs372054960
SNP Nexus

SNPshotrs372054960
SNPdbers372054960
MSV3drs372054960
GWAS Ctlgrs372054960
Max Magnitude0
ClinVar
Risk rs372054960(T;T)
Alt rs372054960(T;T)
Reference rs372054960(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FARS2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.5771526C>T
CLNSRC
CLNACC RCV000198201.1,