rs121909182
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs121909182(C;C) |
Make rs121909182(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 2326027 |
Gene | ABCA3 |
is a | snp |
is | mentioned by |
dbSNP | rs121909182 |
dbSNP (classic) | rs121909182 |
ClinGen | rs121909182 |
ebi | rs121909182 |
HLI | rs121909182 |
Exac | rs121909182 |
Gnomad | rs121909182 |
Varsome | rs121909182 |
LitVar | rs121909182 |
Map | rs121909182 |
PheGenI | rs121909182 |
Biobank | rs121909182 |
1000 genomes | rs121909182 |
hgdp | rs121909182 |
ensembl | rs121909182 |
geneview | rs121909182 |
scholar | rs121909182 |
rs121909182 | |
pharmgkb | rs121909182 |
gwascentral | rs121909182 |
openSNP | rs121909182 |
23andMe | rs121909182 |
SNPshot | rs121909182 |
SNPdbe | rs121909182 |
MSV3d | rs121909182 |
GWAS Ctlg | rs121909182 |
Merged from | Rs28936412 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121909182(C;C) |
Alt | rs121909182(C;C) |
Reference | Rs121909182(T;T) |
Significance | Pathogenic |
Disease | Surfactant metabolism dysfunction |
Variation | info |
Gene | ABCA3 |
CLNDBN | Surfactant metabolism dysfunction, pulmonary, 3 |
Reversed | 1 |
HGVS | NC_000016.9:g.2376028A>G |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000008476.3, |