rs121909344
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs121909344(C;T) |
Make rs121909344(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 74366896 |
Gene | DCTN1 |
is a | snp |
is | mentioned by |
dbSNP | rs121909344 |
dbSNP (classic) | rs121909344 |
ClinGen | rs121909344 |
ebi | rs121909344 |
HLI | rs121909344 |
Exac | rs121909344 |
Gnomad | rs121909344 |
Varsome | rs121909344 |
LitVar | rs121909344 |
Map | rs121909344 |
PheGenI | rs121909344 |
Biobank | rs121909344 |
1000 genomes | rs121909344 |
hgdp | rs121909344 |
ensembl | rs121909344 |
geneview | rs121909344 |
scholar | rs121909344 |
rs121909344 | |
pharmgkb | rs121909344 |
gwascentral | rs121909344 |
openSNP | rs121909344 |
23andMe | rs121909344 |
SNPshot | rs121909344 |
SNPdbe | rs121909344 |
MSV3d | rs121909344 |
GWAS Ctlg | rs121909344 |
Max Magnitude | 0 |
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, |