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rs1057523346

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057523346(C;T)
Make rs1057523346(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position5404575
GeneFARS2
is asnp
is mentioned by
dbSNPrs1057523346
dbSNP (old)rs1057523346
ClinGenrs1057523346
ebirs1057523346
HLIrs1057523346
Exacrs1057523346
Gnomadrs1057523346
Varsomers1057523346
LitVarrs1057523346
Maprs1057523346
PheGenIrs1057523346
Biobankrs1057523346
1000 genomesrs1057523346
hgdprs1057523346
ensemblrs1057523346
gopubmedrs1057523346
geneviewrs1057523346
scholarrs1057523346
googlers1057523346
pharmgkbrs1057523346
gwascentralrs1057523346
openSNPrs1057523346
23andMers1057523346
23andMe allrs1057523346
SNPshotrs1057523346
SNPdbers1057523346
MSV3drs1057523346
GWAS Ctlgrs1057523346
Max Magnitude0
ClinVar
Risk rs1057523346(T;T)
Alt rs1057523346(T;T)
Reference Rs1057523346(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FARS2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.5404808C>T
CLNSRC
CLNACC RCV000418107.1,