Have questions? Visit https://www.reddit.com/r/SNPedia

rs121918207

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918207(A;A)
Make rs121918207(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position173838207
GeneDARS2
is asnp
is mentioned by
dbSNPrs121918207
ebirs121918207
HLIrs121918207
Exacrs121918207
Varsomers121918207
Maprs121918207
PheGenIrs121918207
hapmaprs121918207
1000 genomesrs121918207
hgdprs121918207
ensemblrs121918207
gopubmedrs121918207
geneviewrs121918207
scholarrs121918207
googlers121918207
pharmgkbrs121918207
gwascentralrs121918207
openSNPrs121918207
23andMers121918207
23andMe allrs121918207
SNP Nexus

SNPshotrs121918207
SNPdbers121918207
MSV3drs121918207
GWAS Ctlgrs121918207
Max Magnitude0
OMIM610956
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121918207(A,C;A,C)
Alt rs121918207(A,C;A,C)
Reference rs121918207(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.173807345G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001115.3,