rs760889253
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs760889253(A;A) |
Make rs760889253(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 12 |
Position | 21882807 |
Gene | ABCC9 |
is a | snp |
is | mentioned by |
dbSNP | rs760889253 |
dbSNP (classic) | rs760889253 |
ClinGen | rs760889253 |
ebi | rs760889253 |
HLI | rs760889253 |
Exac | rs760889253 |
Gnomad | rs760889253 |
Varsome | rs760889253 |
LitVar | rs760889253 |
Map | rs760889253 |
PheGenI | rs760889253 |
Biobank | rs760889253 |
1000 genomes | rs760889253 |
hgdp | rs760889253 |
ensembl | rs760889253 |
geneview | rs760889253 |
scholar | rs760889253 |
rs760889253 | |
pharmgkb | rs760889253 |
gwascentral | rs760889253 |
openSNP | rs760889253 |
23andMe | rs760889253 |
SNPshot | rs760889253 |
SNPdbe | rs760889253 |
MSV3d | rs760889253 |
GWAS Ctlg | rs760889253 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs760889253(A;A) |
Alt | rs760889253(A;A) |
Reference | Rs760889253(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ABCC9 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.22035741G>A |
CLNSRC | |
CLNACC | RCV000171209.1, |