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rs121918212

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918212(C;T)
Make rs121918212(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position173857604
GeneDARS2
is asnp
is mentioned by
dbSNPrs121918212
ebirs121918212
HLIrs121918212
Exacrs121918212
Varsomers121918212
Maprs121918212
PheGenIrs121918212
hapmaprs121918212
1000 genomesrs121918212
hgdprs121918212
ensemblrs121918212
gopubmedrs121918212
geneviewrs121918212
scholarrs121918212
googlers121918212
pharmgkbrs121918212
gwascentralrs121918212
openSNPrs121918212
23andMers121918212
23andMe allrs121918212
SNP Nexus

SNPshotrs121918212
SNPdbers121918212
MSV3drs121918212
GWAS Ctlgrs121918212
Max Magnitude0
OMIM610956
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121918212(T;T)
Alt rs121918212(T;T)
Reference rs121918212(C;C)
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.173826742C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001121.3,