rs786205259
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(TTTG;TTTG) | 0 | common in clinvar |
Make rs786205259(-;-) |
Make rs786205259(-;TTTG) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 15 |
Position | 73322592 |
Gene | HCN4 |
is a | snp |
is | mentioned by |
dbSNP | rs786205259 |
dbSNP (classic) | rs786205259 |
ClinGen | rs786205259 |
ebi | rs786205259 |
HLI | rs786205259 |
Exac | rs786205259 |
Gnomad | rs786205259 |
Varsome | rs786205259 |
LitVar | rs786205259 |
Map | rs786205259 |
PheGenI | rs786205259 |
Biobank | rs786205259 |
1000 genomes | rs786205259 |
hgdp | rs786205259 |
ensembl | rs786205259 |
geneview | rs786205259 |
scholar | rs786205259 |
rs786205259 | |
pharmgkb | rs786205259 |
gwascentral | rs786205259 |
openSNP | rs786205259 |
23andMe | rs786205259 |
SNPshot | rs786205259 |
SNPdbe | rs786205259 |
MSV3d | rs786205259 |
GWAS Ctlg | rs786205259 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786205259(-;-) |
Alt | rs786205259(-;-) |
Reference | Rs786205259(TTTG;TTTG) |
Significance | Probable-Pathogenic |
Disease | Sinus node disease |
Variation | info |
Gene | HCN4 |
CLNDBN | Sinus node disease |
Reversed | 1 |
HGVS | NC_000015.9:g.73614933_73614936delCAAA |
CLNSRC | |
CLNACC | RCV000171563.1, |