rs13306668
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs13306668(A;A) |
Make rs13306668(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 16 |
Position | 56879088 |
Gene | SLC12A3 |
is a | snp |
is | mentioned by |
dbSNP | rs13306668 |
dbSNP (classic) | rs13306668 |
ClinGen | rs13306668 |
ebi | rs13306668 |
HLI | rs13306668 |
Exac | rs13306668 |
Gnomad | rs13306668 |
Varsome | rs13306668 |
LitVar | rs13306668 |
Map | rs13306668 |
PheGenI | rs13306668 |
Biobank | rs13306668 |
1000 genomes | rs13306668 |
hgdp | rs13306668 |
ensembl | rs13306668 |
geneview | rs13306668 |
scholar | rs13306668 |
rs13306668 | |
pharmgkb | rs13306668 |
gwascentral | rs13306668 |
openSNP | rs13306668 |
23andMe | rs13306668 |
SNPshot | rs13306668 |
SNPdbe | rs13306668 |
MSV3d | rs13306668 |
GWAS Ctlg | rs13306668 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
ClinVar | |
---|---|
Risk | rs13306668(A;A) rs13306668(C;C) rs13306668(T;T) |
Alt | rs13306668(A;A) rs13306668(C;C) rs13306668(T;T) |
Reference | Rs13306668(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SLC12A3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.56913000G>T |
CLNSRC | |
CLNACC | RCV000439274.1, |