rs121909539
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs121909539(C;G) |
Make rs121909539(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 20693753 |
Gene | ANG, RNASE4 |
is a | snp |
is | mentioned by |
dbSNP | rs121909539 |
dbSNP (classic) | rs121909539 |
ClinGen | rs121909539 |
ebi | rs121909539 |
HLI | rs121909539 |
Exac | rs121909539 |
Gnomad | rs121909539 |
Varsome | rs121909539 |
LitVar | rs121909539 |
Map | rs121909539 |
PheGenI | rs121909539 |
Biobank | rs121909539 |
1000 genomes | rs121909539 |
hgdp | rs121909539 |
ensembl | rs121909539 |
geneview | rs121909539 |
scholar | rs121909539 |
rs121909539 | |
pharmgkb | rs121909539 |
gwascentral | rs121909539 |
openSNP | rs121909539 |
23andMe | rs121909539 |
SNPshot | rs121909539 |
SNPdbe | rs121909539 |
MSV3d | rs121909539 |
GWAS Ctlg | rs121909539 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121909539(G;G) |
Alt | rs121909539(G;G) |
Reference | Rs121909539(C;C) |
Significance | Pathogenic |
Disease | Amyotrophic lateral sclerosis type 9 |
Variation | info |
Gene | RNASE4 ANG |
CLNDBN | Amyotrophic lateral sclerosis type 9 |
Reversed | 0 |
HGVS | NC_000014.8:g.21161912C>G |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000019703.27, |