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rs121909344

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs121909344(C;T)
Make rs121909344(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position74366896
GeneDCTN1
is asnp
is mentioned by
dbSNPrs121909344
ebirs121909344
HLIrs121909344
Exacrs121909344
Varsomers121909344
Maprs121909344
PheGenIrs121909344
hapmaprs121909344
1000 genomesrs121909344
hgdprs121909344
ensemblrs121909344
gopubmedrs121909344
geneviewrs121909344
scholarrs121909344
googlers121909344
pharmgkbrs121909344
gwascentralrs121909344
openSNPrs121909344
23andMers121909344
23andMe allrs121909344
SNP Nexus

SNPshotrs121909344
SNPdbers121909344
MSV3drs121909344
GWAS Ctlgrs121909344
Max Magnitude0
OMIM601143
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121909344(T;T)
Alt rs121909344(T;T)
Reference rs121909344(C;C)
Significance Other
Disease Amyotrophic lateral sclerosis Charcot-Marie-Tooth disease
Variation info
Gene DCTN1
CLNDBN Amyotrophic lateral sclerosis, susceptibility to Charcot-Marie-Tooth disease
Reversed 1
HGVS NC_000002.11:g.74594023G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008912.2, RCV000144867.1,