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rs121918211

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918211(G;T)
Make rs121918211(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position173850408
GeneDARS2
is asnp
is mentioned by
dbSNPrs121918211
ebirs121918211
HLIrs121918211
Exacrs121918211
Varsomers121918211
Maprs121918211
PheGenIrs121918211
hapmaprs121918211
1000 genomesrs121918211
hgdprs121918211
ensemblrs121918211
gopubmedrs121918211
geneviewrs121918211
scholarrs121918211
googlers121918211
pharmgkbrs121918211
gwascentralrs121918211
openSNPrs121918211
23andMers121918211
23andMe allrs121918211
SNP Nexus

SNPshotrs121918211
SNPdbers121918211
MSV3drs121918211
GWAS Ctlgrs121918211
Max Magnitude0
OMIM610956
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121918211(T;T)
Alt rs121918211(T;T)
Reference rs121918211(G;G)
Significance Pathogenic
Disease Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation
Variation info
Gene DARS2
CLNDBN Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation
Reversed 0
HGVS NC_000001.10:g.173819546G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001120.3,