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rs121909343

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs121909343(C;C)
Make rs121909343(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position74368870
GeneDCTN1
is asnp
is mentioned by
dbSNPrs121909343
ebirs121909343
HLIrs121909343
Exacrs121909343
Varsomers121909343
Maprs121909343
PheGenIrs121909343
hapmaprs121909343
1000 genomesrs121909343
hgdprs121909343
ensemblrs121909343
gopubmedrs121909343
geneviewrs121909343
scholarrs121909343
googlers121909343
pharmgkbrs121909343
gwascentralrs121909343
openSNPrs121909343
23andMers121909343
23andMe allrs121909343
SNP Nexus

SNPshotrs121909343
SNPdbers121909343
MSV3drs121909343
GWAS Ctlgrs121909343
Max Magnitude0
OMIM601143
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121909343(C;C)
Alt rs121909343(C;C)
Reference rs121909343(T;T)
Significance Other
Disease Amyotrophic lateral sclerosis
Variation info
Gene DCTN1
CLNDBN Amyotrophic lateral sclerosis, susceptibility to
Reversed 1
HGVS NC_000002.11:g.74595997A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000008911.2,