rs750349088
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs750349088(A;A) |
Make rs750349088(A;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 21 |
Position | 34449373 |
Gene | KCNE1 |
is a | snp |
is | mentioned by |
dbSNP | rs750349088 |
dbSNP (classic) | rs750349088 |
ClinGen | rs750349088 |
ebi | rs750349088 |
HLI | rs750349088 |
Exac | rs750349088 |
Gnomad | rs750349088 |
Varsome | rs750349088 |
LitVar | rs750349088 |
Map | rs750349088 |
PheGenI | rs750349088 |
Biobank | rs750349088 |
1000 genomes | rs750349088 |
hgdp | rs750349088 |
ensembl | rs750349088 |
geneview | rs750349088 |
scholar | rs750349088 |
rs750349088 | |
pharmgkb | rs750349088 |
gwascentral | rs750349088 |
openSNP | rs750349088 |
23andMe | rs750349088 |
SNPshot | rs750349088 |
SNPdbe | rs750349088 |
MSV3d | rs750349088 |
GWAS Ctlg | rs750349088 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs750349088(A;A) rs750349088(T;T) |
Alt | rs750349088(A;A) rs750349088(T;T) |
Reference | Rs750349088(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | KCNE1B KCNE1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000021.8:g.35821671G>A |
CLNSRC | |
CLNACC | RCV000256077.1, |