rs886037850
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs886037850(A;A) |
Make rs886037850(A;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 16 |
Position | 31484885 |
Gene | SLC5A2 |
is a | snp |
is | mentioned by |
dbSNP | rs886037850 |
dbSNP (classic) | rs886037850 |
ClinGen | rs886037850 |
ebi | rs886037850 |
HLI | rs886037850 |
Exac | rs886037850 |
Gnomad | rs886037850 |
Varsome | rs886037850 |
LitVar | rs886037850 |
Map | rs886037850 |
PheGenI | rs886037850 |
Biobank | rs886037850 |
1000 genomes | rs886037850 |
hgdp | rs886037850 |
ensembl | rs886037850 |
geneview | rs886037850 |
scholar | rs886037850 |
rs886037850 | |
pharmgkb | rs886037850 |
gwascentral | rs886037850 |
openSNP | rs886037850 |
23andMe | rs886037850 |
SNPshot | rs886037850 |
SNPdbe | rs886037850 |
MSV3d | rs886037850 |
GWAS Ctlg | rs886037850 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886037850(A;A) |
Alt | rs886037850(A;A) |
Reference | Rs886037850(G;G) |
Significance | Pathogenic |
Disease | Familial renal glucosuria |
Variation | info |
Gene | SLC5A2 |
CLNDBN | Familial renal glucosuria |
Reversed | 0 |
HGVS | NC_000016.9:g.31496206G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000239563.1, |