rs762610288
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs762610288(A;A) |
Make rs762610288(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 9 |
Position | 137236239 |
Gene | SLC34A3 |
is a | snp |
is | mentioned by |
dbSNP | rs762610288 |
dbSNP (classic) | rs762610288 |
ClinGen | rs762610288 |
ebi | rs762610288 |
HLI | rs762610288 |
Exac | rs762610288 |
Gnomad | rs762610288 |
Varsome | rs762610288 |
LitVar | rs762610288 |
Map | rs762610288 |
PheGenI | rs762610288 |
Biobank | rs762610288 |
1000 genomes | rs762610288 |
hgdp | rs762610288 |
ensembl | rs762610288 |
geneview | rs762610288 |
scholar | rs762610288 |
rs762610288 | |
pharmgkb | rs762610288 |
gwascentral | rs762610288 |
openSNP | rs762610288 |
23andMe | rs762610288 |
SNPshot | rs762610288 |
SNPdbe | rs762610288 |
MSV3d | rs762610288 |
GWAS Ctlg | rs762610288 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs762610288(A;A) |
Alt | rs762610288(A;A) |
Reference | Rs762610288(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SLC34A3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.140130691G>A |
CLNSRC | |
CLNACC | RCV000484421.1, |