rs200247956
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs200247956(A;A) |
Make rs200247956(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 42929655 |
Gene | SLC2A1 |
is a | snp |
is | mentioned by |
dbSNP | rs200247956 |
dbSNP (classic) | rs200247956 |
ClinGen | rs200247956 |
ebi | rs200247956 |
HLI | rs200247956 |
Exac | rs200247956 |
Gnomad | rs200247956 |
Varsome | rs200247956 |
LitVar | rs200247956 |
Map | rs200247956 |
PheGenI | rs200247956 |
Biobank | rs200247956 |
1000 genomes | rs200247956 |
hgdp | rs200247956 |
ensembl | rs200247956 |
geneview | rs200247956 |
scholar | rs200247956 |
rs200247956 | |
pharmgkb | rs200247956 |
gwascentral | rs200247956 |
openSNP | rs200247956 |
23andMe | rs200247956 |
SNPshot | rs200247956 |
SNPdbe | rs200247956 |
MSV3d | rs200247956 |
GWAS Ctlg | rs200247956 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs200247956(A;A) |
Alt | rs200247956(A;A) |
Reference | Rs200247956(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SLC2A1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.43395326G>A |
CLNSRC | |
CLNACC | RCV000189396.1, |