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rs1057520702

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520702(A;A)
Make rs1057520702(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position220138044
GeneIARS2
is asnp
is mentioned by
dbSNPrs1057520702
dbSNP (old)rs1057520702
ClinGenrs1057520702
ebirs1057520702
HLIrs1057520702
Exacrs1057520702
Gnomadrs1057520702
Varsomers1057520702
Maprs1057520702
PheGenIrs1057520702
Biobankrs1057520702
1000 genomesrs1057520702
hgdprs1057520702
ensemblrs1057520702
gopubmedrs1057520702
geneviewrs1057520702
scholarrs1057520702
googlers1057520702
pharmgkbrs1057520702
gwascentralrs1057520702
openSNPrs1057520702
23andMers1057520702
23andMe allrs1057520702
SNPshotrs1057520702
SNPdbers1057520702
MSV3drs1057520702
GWAS Ctlgrs1057520702
Max Magnitude0
ClinVar
Risk rs1057520702(A;A)
Alt rs1057520702(A;A)
Reference Rs1057520702(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene IARS2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.220311386G>A
CLNSRC
CLNACC RCV000429997.1,