rs761721442
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs761721442(A;A) |
Make rs761721442(A;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 20 |
Position | 46726988 |
Gene | SLC2A10 |
is a | snp |
is | mentioned by |
dbSNP | rs761721442 |
dbSNP (classic) | rs761721442 |
ClinGen | rs761721442 |
ebi | rs761721442 |
HLI | rs761721442 |
Exac | rs761721442 |
Gnomad | rs761721442 |
Varsome | rs761721442 |
LitVar | rs761721442 |
Map | rs761721442 |
PheGenI | rs761721442 |
Biobank | rs761721442 |
1000 genomes | rs761721442 |
hgdp | rs761721442 |
ensembl | rs761721442 |
geneview | rs761721442 |
scholar | rs761721442 |
rs761721442 | |
pharmgkb | rs761721442 |
gwascentral | rs761721442 |
openSNP | rs761721442 |
23andMe | rs761721442 |
SNPshot | rs761721442 |
SNPdbe | rs761721442 |
MSV3d | rs761721442 |
GWAS Ctlg | rs761721442 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs761721442(A;A) |
Alt | rs761721442(A;A) |
Reference | Rs761721442(T;T) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SLC2A10 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000020.10:g.45355627T>A |
CLNSRC | |
CLNACC | RCV000197685.1, |