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rs143722284

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs143722284(A;A)
Make rs143722284(A;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position220137990
GeneIARS2
is asnp
is mentioned by
dbSNPrs143722284
ebirs143722284
HLIrs143722284
Exacrs143722284
Varsomers143722284
Maprs143722284
PheGenIrs143722284
hapmaprs143722284
1000 genomesrs143722284
hgdprs143722284
ensemblrs143722284
gopubmedrs143722284
geneviewrs143722284
scholarrs143722284
googlers143722284
pharmgkbrs143722284
gwascentralrs143722284
openSNPrs143722284
23andMers143722284
23andMe allrs143722284
SNP Nexus

SNPshotrs143722284
SNPdbers143722284
MSV3drs143722284
GWAS Ctlgrs143722284
Max Magnitude0
ClinVar
Risk rs143722284(A;A)
Alt rs143722284(A;A)
Reference rs143722284(G;G)
Significance Pathogenic
Disease Leigh syndrome not provided
Variation info
Gene IARS2
CLNDBN Leigh syndrome not provided
Reversed 0
HGVS NC_000001.10:g.220311332G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000144717.1, RCV000144956.3,