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rs121909345

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121909345(A;A)
Make rs121909345(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position74363337
GeneDCTN1
is asnp
is mentioned by
dbSNPrs121909345
ebirs121909345
HLIrs121909345
Exacrs121909345
Varsomers121909345
Maprs121909345
PheGenIrs121909345
hapmaprs121909345
1000 genomesrs121909345
hgdprs121909345
ensemblrs121909345
gopubmedrs121909345
geneviewrs121909345
scholarrs121909345
googlers121909345
pharmgkbrs121909345
gwascentralrs121909345
openSNPrs121909345
23andMers121909345
23andMe allrs121909345
SNP Nexus

SNPshotrs121909345
SNPdbers121909345
MSV3drs121909345
GWAS Ctlgrs121909345
Max Magnitude0
OMIM601143
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121909345(A;A)
Alt rs121909345(A;A)
Reference rs121909345(G;G)
Significance Other
Disease Amyotrophic lateral sclerosis
Variation info
Gene DCTN1
CLNDBN Amyotrophic lateral sclerosis, susceptibility to
Reversed 1
HGVS NC_000002.11:g.74590464C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008913.2,