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rs374957295

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs374957295(C;T)
Make rs374957295(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position5368893
GeneFARS2
is asnp
is mentioned by
dbSNPrs374957295
ebirs374957295
HLIrs374957295
Exacrs374957295
Varsomers374957295
Maprs374957295
PheGenIrs374957295
hapmaprs374957295
1000 genomesrs374957295
hgdprs374957295
ensemblrs374957295
gopubmedrs374957295
geneviewrs374957295
scholarrs374957295
googlers374957295
pharmgkbrs374957295
gwascentralrs374957295
openSNPrs374957295
23andMers374957295
23andMe allrs374957295
SNP Nexus

SNPshotrs374957295
SNPdbers374957295
MSV3drs374957295
GWAS Ctlgrs374957295
Max Magnitude0
ClinVar
Risk rs374957295(G,T;G,T)
Alt rs374957295(G,T;G,T)
Reference rs374957295(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FARS2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.5369126C>T
CLNSRC
CLNACC RCV000199836.1,