rs281864791
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(ATTT;ATTT) | 0 | common in clinvar |
(I;I) | 0 | common genotype |
(TTAT;TTAT) | 0 | common in clinvar |
Make rs281864791(-;-) |
Make rs281864791(-;TTAT) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 68525822 |
Gene | PRKAR1A |
is a | snp |
is | mentioned by |
dbSNP | rs281864791 |
dbSNP (classic) | rs281864791 |
ClinGen | rs281864791 |
ebi | rs281864791 |
HLI | rs281864791 |
Exac | rs281864791 |
Gnomad | rs281864791 |
Varsome | rs281864791 |
LitVar | rs281864791 |
Map | rs281864791 |
PheGenI | rs281864791 |
Biobank | rs281864791 |
1000 genomes | rs281864791 |
hgdp | rs281864791 |
ensembl | rs281864791 |
geneview | rs281864791 |
scholar | rs281864791 |
rs281864791 | |
pharmgkb | rs281864791 |
gwascentral | rs281864791 |
openSNP | rs281864791 |
23andMe | rs281864791 |
SNPshot | rs281864791 |
SNPdbe | rs281864791 |
MSV3d | rs281864791 |
GWAS Ctlg | rs281864791 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs281864791(-;-) |
Alt | rs281864791(-;-) |
Reference | Rs281864791(ATTT;ATTT) |
Significance | Pathogenic |
Disease | Atrial myxoma |
Variation | info |
Gene | PRKAR1A |
CLNDBN | Atrial myxoma, familial |
Reversed | 0 |
HGVS | NC_000017.10:g.66521963_66521966delTTAT |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000013501.18, |