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rs1057522050

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057522050(C;C)
Make rs1057522050(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position87514991
GeneRARS2
is asnp
is mentioned by
dbSNPrs1057522050
dbSNP (old)rs1057522050
ClinGenrs1057522050
ebirs1057522050
HLIrs1057522050
Exacrs1057522050
Gnomadrs1057522050
Varsomers1057522050
Maprs1057522050
PheGenIrs1057522050
Biobankrs1057522050
1000 genomesrs1057522050
hgdprs1057522050
ensemblrs1057522050
gopubmedrs1057522050
geneviewrs1057522050
scholarrs1057522050
googlers1057522050
pharmgkbrs1057522050
gwascentralrs1057522050
openSNPrs1057522050
23andMers1057522050
23andMe allrs1057522050
SNPshotrs1057522050
SNPdbers1057522050
MSV3drs1057522050
GWAS Ctlgrs1057522050
Max Magnitude0
ClinVar
Risk rs1057522050(C;C)
Alt rs1057522050(C;C)
Reference Rs1057522050(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RARS2
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.88224709A>G
CLNSRC
CLNACC RCV000417917.1,