rs61757261
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs61757261(G;G) |
Make rs61757261(G;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 11847373 |
Gene | NPPA, NPPA-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs61757261 |
dbSNP (classic) | rs61757261 |
ClinGen | rs61757261 |
ebi | rs61757261 |
HLI | rs61757261 |
Exac | rs61757261 |
Gnomad | rs61757261 |
Varsome | rs61757261 |
LitVar | rs61757261 |
Map | rs61757261 |
PheGenI | rs61757261 |
Biobank | rs61757261 |
1000 genomes | rs61757261 |
hgdp | rs61757261 |
ensembl | rs61757261 |
geneview | rs61757261 |
scholar | rs61757261 |
rs61757261 | |
pharmgkb | rs61757261 |
gwascentral | rs61757261 |
openSNP | rs61757261 |
23andMe | rs61757261 |
SNPshot | rs61757261 |
SNPdbe | rs61757261 |
MSV3d | rs61757261 |
GWAS Ctlg | rs61757261 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs61757261(G;G) |
Alt | rs61757261(G;G) |
Reference | Rs61757261(T;T) |
Significance | Other |
Disease | Atrial fibrillation |
Variation | info |
Gene | NPPA NPPA-AS1 |
CLNDBN | Atrial fibrillation, familial, 6 |
Reversed | 0 |
HGVS | NC_000001.10:g.11907430T>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000114741.4, |