rs587776851
From SNPedia
Orientation | plus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(AA;AA) | 0 | common in clinvar |
(AAG;AAG) | 0 | common in clinvar |
(I;I) | 0 | common genotype |
(TT;TT) | 0 | common in clinvar |
Make rs587776851(-;-) |
Make rs587776851(-;TT) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 11846008 |
Gene | NPPA-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs587776851 |
dbSNP (classic) | rs587776851 |
ClinGen | rs587776851 |
ebi | rs587776851 |
HLI | rs587776851 |
Exac | rs587776851 |
Gnomad | rs587776851 |
Varsome | rs587776851 |
LitVar | rs587776851 |
Map | rs587776851 |
PheGenI | rs587776851 |
Biobank | rs587776851 |
1000 genomes | rs587776851 |
hgdp | rs587776851 |
ensembl | rs587776851 |
geneview | rs587776851 |
scholar | rs587776851 |
rs587776851 | |
pharmgkb | rs587776851 |
gwascentral | rs587776851 |
openSNP | rs587776851 |
23andMe | rs587776851 |
SNPshot | rs587776851 |
SNPdbe | rs587776851 |
MSV3d | rs587776851 |
GWAS Ctlg | rs587776851 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | Rs587776851(TT;TT) rs587776851(-;-) |
Alt | Rs587776851(TT;TT) rs587776851(-;-) |
Reference | Rs587776851(AA;AA) |
Significance | Pathogenic |
Disease | Atrial fibrillation |
Variation | info |
Gene | NPPA-AS1 |
CLNDBN | Atrial fibrillation, familial, 6 |
Reversed | 1 |
HGVS | NC_000001.10:g.11906065_11906066delTT |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000019366.23, |