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rs121918209

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121918209(A;G)
Make rs121918209(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position173826692
GeneDARS2
is asnp
is mentioned by
dbSNPrs121918209
ebirs121918209
HLIrs121918209
Exacrs121918209
Varsomers121918209
Maprs121918209
PheGenIrs121918209
hapmaprs121918209
1000 genomesrs121918209
hgdprs121918209
ensemblrs121918209
gopubmedrs121918209
geneviewrs121918209
scholarrs121918209
googlers121918209
pharmgkbrs121918209
gwascentralrs121918209
openSNPrs121918209
23andMers121918209
23andMe allrs121918209
SNP Nexus

SNPshotrs121918209
SNPdbers121918209
MSV3drs121918209
GWAS Ctlgrs121918209
Max Magnitude0
OMIM610956
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121918209(G;G)
Alt rs121918209(G;G)
Reference rs121918209(A;A)
Significance Pathogenic
Disease Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation
Variation info
Gene DARS2 CENPL
CLNDBN Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation
Reversed 0
HGVS NC_000001.10:g.173795830A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000001118.3,