rs752514808
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs752514808(C;T) |
Make rs752514808(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 9 |
Position | 135765061 |
Gene | KCNT1 |
is a | snp |
is | mentioned by |
dbSNP | rs752514808 |
dbSNP (classic) | rs752514808 |
ClinGen | rs752514808 |
ebi | rs752514808 |
HLI | rs752514808 |
Exac | rs752514808 |
Gnomad | rs752514808 |
Varsome | rs752514808 |
LitVar | rs752514808 |
Map | rs752514808 |
PheGenI | rs752514808 |
Biobank | rs752514808 |
1000 genomes | rs752514808 |
hgdp | rs752514808 |
ensembl | rs752514808 |
geneview | rs752514808 |
scholar | rs752514808 |
rs752514808 | |
pharmgkb | rs752514808 |
gwascentral | rs752514808 |
openSNP | rs752514808 |
23andMe | rs752514808 |
SNPshot | rs752514808 |
SNPdbe | rs752514808 |
MSV3d | rs752514808 |
GWAS Ctlg | rs752514808 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs752514808(G;G) rs752514808(T;T) |
Alt | rs752514808(G;G) rs752514808(T;T) |
Reference | Rs752514808(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | KCNT1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.138656907C>T |
CLNSRC | |
CLNACC | RCV000420451.1, |