rs149955375
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs149955375(A;A) |
Make rs149955375(A;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 7 |
Position | 150947623 |
Gene | KCNH2 |
is a | snp |
is | mentioned by |
dbSNP | rs149955375 |
dbSNP (classic) | rs149955375 |
ClinGen | rs149955375 |
ebi | rs149955375 |
HLI | rs149955375 |
Exac | rs149955375 |
Gnomad | rs149955375 |
Varsome | rs149955375 |
LitVar | rs149955375 |
Map | rs149955375 |
PheGenI | rs149955375 |
Biobank | rs149955375 |
1000 genomes | rs149955375 |
hgdp | rs149955375 |
ensembl | rs149955375 |
geneview | rs149955375 |
scholar | rs149955375 |
rs149955375 | |
pharmgkb | rs149955375 |
gwascentral | rs149955375 |
openSNP | rs149955375 |
23andMe | rs149955375 |
SNPshot | rs149955375 |
SNPdbe | rs149955375 |
MSV3d | rs149955375 |
GWAS Ctlg | rs149955375 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs149955375(A;A) |
Alt | rs149955375(A;A) |
Reference | Rs149955375(G;G) |
Significance | Other |
Disease | Congenital long QT syndrome Long QT syndrome not specified |
Variation | info |
Gene | KCNH2 |
CLNDBN | Congenital long QT syndrome Long QT syndrome not specified |
Reversed | 0 |
HGVS | NC_000007.13:g.150644711G>A |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000058182.3, RCV000148532.4, RCV000181901.5, |