rs373890183
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs373890183(A;A) |
Make rs373890183(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 12 |
Position | 21848201 |
Gene | ABCC9 |
is a | snp |
is | mentioned by |
dbSNP | rs373890183 |
dbSNP (classic) | rs373890183 |
ClinGen | rs373890183 |
ebi | rs373890183 |
HLI | rs373890183 |
Exac | rs373890183 |
Gnomad | rs373890183 |
Varsome | rs373890183 |
LitVar | rs373890183 |
Map | rs373890183 |
PheGenI | rs373890183 |
Biobank | rs373890183 |
1000 genomes | rs373890183 |
hgdp | rs373890183 |
ensembl | rs373890183 |
geneview | rs373890183 |
scholar | rs373890183 |
rs373890183 | |
pharmgkb | rs373890183 |
gwascentral | rs373890183 |
openSNP | rs373890183 |
23andMe | rs373890183 |
SNPshot | rs373890183 |
SNPdbe | rs373890183 |
MSV3d | rs373890183 |
GWAS Ctlg | rs373890183 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs373890183(A;A) |
Alt | rs373890183(A;A) |
Reference | Rs373890183(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ABCC9 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.22001135G>A |
CLNSRC | |
CLNACC | RCV000171208.1, |