rs373901523
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs373901523(G;T) |
Make rs373901523(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 16 |
Position | 56887932 |
Gene | SLC12A3 |
is a | snp |
is | mentioned by |
dbSNP | rs373901523 |
dbSNP (classic) | rs373901523 |
ClinGen | rs373901523 |
ebi | rs373901523 |
HLI | rs373901523 |
Exac | rs373901523 |
Gnomad | rs373901523 |
Varsome | rs373901523 |
LitVar | rs373901523 |
Map | rs373901523 |
PheGenI | rs373901523 |
Biobank | rs373901523 |
1000 genomes | rs373901523 |
hgdp | rs373901523 |
ensembl | rs373901523 |
geneview | rs373901523 |
scholar | rs373901523 |
rs373901523 | |
pharmgkb | rs373901523 |
gwascentral | rs373901523 |
openSNP | rs373901523 |
23andMe | rs373901523 |
SNPshot | rs373901523 |
SNPdbe | rs373901523 |
MSV3d | rs373901523 |
GWAS Ctlg | rs373901523 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs373901523(A;A) rs373901523(T;T) |
Alt | rs373901523(A;A) rs373901523(T;T) |
Reference | Rs373901523(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SLC12A3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.56921844G>A |
CLNSRC | |
CLNACC | RCV000412838.1, |