rs397517184
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs397517184(C;C) |
Make rs397517184(C;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 12 |
Position | 21906141 |
Gene | ABCC9 |
is a | snp |
is | mentioned by |
dbSNP | rs397517184 |
dbSNP (classic) | rs397517184 |
ClinGen | rs397517184 |
ebi | rs397517184 |
HLI | rs397517184 |
Exac | rs397517184 |
Gnomad | rs397517184 |
Varsome | rs397517184 |
LitVar | rs397517184 |
Map | rs397517184 |
PheGenI | rs397517184 |
Biobank | rs397517184 |
1000 genomes | rs397517184 |
hgdp | rs397517184 |
ensembl | rs397517184 |
geneview | rs397517184 |
scholar | rs397517184 |
rs397517184 | |
pharmgkb | rs397517184 |
gwascentral | rs397517184 |
openSNP | rs397517184 |
23andMe | rs397517184 |
SNPshot | rs397517184 |
SNPdbe | rs397517184 |
MSV3d | rs397517184 |
GWAS Ctlg | rs397517184 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs397517184(C;C) |
Alt | rs397517184(C;C) |
Reference | Rs397517184(T;T) |
Significance | Other |
Disease | not specified |
Variation | info |
Gene | ABCC9 |
CLNDBN | not specified |
Reversed | 1 |
HGVS | NC_000012.11:g.22059075A>G |
CLNSRC | |
CLNACC | RCV000038586.4, |