rs752143706
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs752143706(C;T) |
Make rs752143706(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 42927147 |
Gene | SLC2A1 |
is a | snp |
is | mentioned by |
dbSNP | rs752143706 |
dbSNP (classic) | rs752143706 |
ClinGen | rs752143706 |
ebi | rs752143706 |
HLI | rs752143706 |
Exac | rs752143706 |
Gnomad | rs752143706 |
Varsome | rs752143706 |
LitVar | rs752143706 |
Map | rs752143706 |
PheGenI | rs752143706 |
Biobank | rs752143706 |
1000 genomes | rs752143706 |
hgdp | rs752143706 |
ensembl | rs752143706 |
geneview | rs752143706 |
scholar | rs752143706 |
rs752143706 | |
pharmgkb | rs752143706 |
gwascentral | rs752143706 |
openSNP | rs752143706 |
23andMe | rs752143706 |
SNPshot | rs752143706 |
SNPdbe | rs752143706 |
MSV3d | rs752143706 |
GWAS Ctlg | rs752143706 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs752143706(T;T) |
Alt | rs752143706(T;T) |
Reference | Rs752143706(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SLC2A1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.43392818C>T |
CLNSRC | |
CLNACC | RCV000440623.1, |