rs41310749
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs41310749(A;A) |
Make rs41310749(A;G) |
Make rs41310749(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 38651526 |
Gene | SCN5A |
is a | snp |
is | mentioned by |
dbSNP | rs41310749 |
dbSNP (classic) | rs41310749 |
ClinGen | rs41310749 |
ebi | rs41310749 |
HLI | rs41310749 |
Exac | rs41310749 |
Gnomad | rs41310749 |
Varsome | rs41310749 |
LitVar | rs41310749 |
Map | rs41310749 |
PheGenI | rs41310749 |
Biobank | rs41310749 |
1000 genomes | rs41310749 |
hgdp | rs41310749 |
ensembl | rs41310749 |
geneview | rs41310749 |
scholar | rs41310749 |
rs41310749 | |
pharmgkb | rs41310749 |
gwascentral | rs41310749 |
openSNP | rs41310749 |
23andMe | rs41310749 |
SNPshot | rs41310749 |
SNPdbe | rs41310749 |
MSV3d | rs41310749 |
GWAS Ctlg | rs41310749 |
GMAF | 0.14 |
Max Magnitude | 0 |
[PMID 22370247] Genetic variants in SCN5A promoter are associated with arrhythmia phenotype severity in patients with heterozygous loss of function mutation