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rs587776985

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587776985(C;T)
Make rs587776985(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position135911174
GeneDARS
is asnp
is mentioned by
dbSNPrs587776985
ebirs587776985
HLIrs587776985
Exacrs587776985
Varsomers587776985
Maprs587776985
PheGenIrs587776985
hapmaprs587776985
1000 genomesrs587776985
hgdprs587776985
ensemblrs587776985
gopubmedrs587776985
geneviewrs587776985
scholarrs587776985
googlers587776985
pharmgkbrs587776985
gwascentralrs587776985
openSNPrs587776985
23andMers587776985
23andMe allrs587776985
SNP Nexus

SNPshotrs587776985
SNPdbers587776985
MSV3drs587776985
GWAS Ctlgrs587776985
Max Magnitude0
ClinVar
Risk rs587776985(T;T)
Alt rs587776985(T;T)
Reference rs587776985(C;C)
Significance Pathogenic
Disease Hypomyelination with brainstem and spinal cord involvement and leg spasticity
Variation info
Gene DARS
CLNDBN Hypomyelination with brainstem and spinal cord involvement and leg spasticity
Reversed 0
HGVS NC_000002.11:g.136668744C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000043686.3,