rs794728437
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(TAC;TAC) | 0 | common in clinvar |
Make rs794728437(-;-) |
Make rs794728437(-;TAC) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 7 |
Position | 150952557 |
Gene | KCNH2 |
is a | snp |
is | mentioned by |
dbSNP | rs794728437 |
dbSNP (classic) | rs794728437 |
ClinGen | rs794728437 |
ebi | rs794728437 |
HLI | rs794728437 |
Exac | rs794728437 |
Gnomad | rs794728437 |
Varsome | rs794728437 |
LitVar | rs794728437 |
Map | rs794728437 |
PheGenI | rs794728437 |
Biobank | rs794728437 |
1000 genomes | rs794728437 |
hgdp | rs794728437 |
ensembl | rs794728437 |
geneview | rs794728437 |
scholar | rs794728437 |
rs794728437 | |
pharmgkb | rs794728437 |
gwascentral | rs794728437 |
openSNP | rs794728437 |
23andMe | rs794728437 |
SNPshot | rs794728437 |
SNPdbe | rs794728437 |
MSV3d | rs794728437 |
GWAS Ctlg | rs794728437 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs794728437(-;-) |
Alt | rs794728437(-;-) |
Reference | Rs794728437(TAC;TAC) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | KCNH2 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000007.13:g.150649645_150649647delGTA |
CLNSRC | |
CLNACC | RCV000181975.2, |