rs121909540
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs121909540(A;T) |
Make rs121909540(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 20693755 |
Gene | ANG, RNASE4 |
is a | snp |
is | mentioned by |
dbSNP | rs121909540 |
dbSNP (classic) | rs121909540 |
ClinGen | rs121909540 |
ebi | rs121909540 |
HLI | rs121909540 |
Exac | rs121909540 |
Gnomad | rs121909540 |
Varsome | rs121909540 |
LitVar | rs121909540 |
Map | rs121909540 |
PheGenI | rs121909540 |
Biobank | rs121909540 |
1000 genomes | rs121909540 |
hgdp | rs121909540 |
ensembl | rs121909540 |
geneview | rs121909540 |
scholar | rs121909540 |
rs121909540 | |
pharmgkb | rs121909540 |
gwascentral | rs121909540 |
openSNP | rs121909540 |
23andMe | rs121909540 |
SNPshot | rs121909540 |
SNPdbe | rs121909540 |
MSV3d | rs121909540 |
GWAS Ctlg | rs121909540 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121909540(T;T) |
Alt | rs121909540(T;T) |
Reference | Rs121909540(A;A) |
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.21161914A>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000019704.26, |