rs763130915
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(ACG;ACG) | 0 | common in clinvar |
Make rs763130915(-;-) |
Make rs763130915(-;ACG) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 227699210 |
Gene | SLC19A3 |
is a | snp |
is | mentioned by |
dbSNP | rs763130915 |
dbSNP (classic) | rs763130915 |
ClinGen | rs763130915 |
ebi | rs763130915 |
HLI | rs763130915 |
Exac | rs763130915 |
Gnomad | rs763130915 |
Varsome | rs763130915 |
LitVar | rs763130915 |
Map | rs763130915 |
PheGenI | rs763130915 |
Biobank | rs763130915 |
1000 genomes | rs763130915 |
hgdp | rs763130915 |
ensembl | rs763130915 |
geneview | rs763130915 |
scholar | rs763130915 |
rs763130915 | |
pharmgkb | rs763130915 |
gwascentral | rs763130915 |
openSNP | rs763130915 |
23andMe | rs763130915 |
SNPshot | rs763130915 |
SNPdbe | rs763130915 |
MSV3d | rs763130915 |
GWAS Ctlg | rs763130915 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs763130915(-;-) |
Alt | rs763130915(-;-) |
Reference | Rs763130915(ACG;ACG) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SLC19A3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.228563926_228563928delACG |
CLNSRC | |
CLNACC | RCV000486999.1, |