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rs373436822

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs373436822(A;A)
Make rs373436822(A;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position220126827
GeneIARS2
is asnp
is mentioned by
dbSNPrs373436822
ebirs373436822
HLIrs373436822
Exacrs373436822
Varsomers373436822
Maprs373436822
PheGenIrs373436822
hapmaprs373436822
1000 genomesrs373436822
hgdprs373436822
ensemblrs373436822
gopubmedrs373436822
geneviewrs373436822
scholarrs373436822
googlers373436822
pharmgkbrs373436822
gwascentralrs373436822
openSNPrs373436822
23andMers373436822
23andMe allrs373436822
SNP Nexus

SNPshotrs373436822
SNPdbers373436822
MSV3drs373436822
GWAS Ctlgrs373436822
Max Magnitude0
ClinVar
Risk rs373436822(A;A)
Alt rs373436822(A;A)
Reference rs373436822(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.220300169G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000144716.1, RCV000144955.3,