rs886039182
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs886039182(-;A) |
Make rs886039182(A;A) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 10 |
Position | 119676846 |
Gene | BAG3 |
is a | snp |
is | mentioned by |
dbSNP | rs886039182 |
dbSNP (classic) | rs886039182 |
ClinGen | rs886039182 |
ebi | rs886039182 |
HLI | rs886039182 |
Exac | rs886039182 |
Gnomad | rs886039182 |
Varsome | rs886039182 |
LitVar | rs886039182 |
Map | rs886039182 |
PheGenI | rs886039182 |
Biobank | rs886039182 |
1000 genomes | rs886039182 |
hgdp | rs886039182 |
ensembl | rs886039182 |
geneview | rs886039182 |
scholar | rs886039182 |
rs886039182 | |
pharmgkb | rs886039182 |
gwascentral | rs886039182 |
openSNP | rs886039182 |
23andMe | rs886039182 |
SNPshot | rs886039182 |
SNPdbe | rs886039182 |
MSV3d | rs886039182 |
GWAS Ctlg | rs886039182 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886039182(A;A) |
Alt | rs886039182(A;A) |
Reference | Rs886039182(-;-) |
Significance | Pathogenic |
Disease | Cardiovascular phenotype |
Variation | info |
Gene | BAG3 |
CLNDBN | Cardiovascular phenotype |
Reversed | 0 |
HGVS | NC_000010.10:g.121436358dupA |
CLNSRC | |
CLNACC | RCV000252646.1, |