rs748547209
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs748547209(A;T) |
Make rs748547209(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 16 |
Position | 56868327 |
Gene | SLC12A3 |
is a | snp |
is | mentioned by |
dbSNP | rs748547209 |
dbSNP (classic) | rs748547209 |
ClinGen | rs748547209 |
ebi | rs748547209 |
HLI | rs748547209 |
Exac | rs748547209 |
Gnomad | rs748547209 |
Varsome | rs748547209 |
LitVar | rs748547209 |
Map | rs748547209 |
PheGenI | rs748547209 |
Biobank | rs748547209 |
1000 genomes | rs748547209 |
hgdp | rs748547209 |
ensembl | rs748547209 |
geneview | rs748547209 |
scholar | rs748547209 |
rs748547209 | |
pharmgkb | rs748547209 |
gwascentral | rs748547209 |
openSNP | rs748547209 |
23andMe | rs748547209 |
SNPshot | rs748547209 |
SNPdbe | rs748547209 |
MSV3d | rs748547209 |
GWAS Ctlg | rs748547209 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs748547209(T;T) |
Alt | rs748547209(T;T) |
Reference | Rs748547209(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SLC12A3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.56902239A>T |
CLNSRC | |
CLNACC | RCV000493117.1, |