rs200679026
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs200679026(A;A) |
Make rs200679026(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 9 |
Position | 94605552 |
Gene | FBP1 |
is a | snp |
is | mentioned by |
dbSNP | rs200679026 |
dbSNP (classic) | rs200679026 |
ClinGen | rs200679026 |
ebi | rs200679026 |
HLI | rs200679026 |
Exac | rs200679026 |
Gnomad | rs200679026 |
Varsome | rs200679026 |
LitVar | rs200679026 |
Map | rs200679026 |
PheGenI | rs200679026 |
Biobank | rs200679026 |
1000 genomes | rs200679026 |
hgdp | rs200679026 |
ensembl | rs200679026 |
geneview | rs200679026 |
scholar | rs200679026 |
rs200679026 | |
pharmgkb | rs200679026 |
gwascentral | rs200679026 |
openSNP | rs200679026 |
23andMe | rs200679026 |
SNPshot | rs200679026 |
SNPdbe | rs200679026 |
MSV3d | rs200679026 |
GWAS Ctlg | rs200679026 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs200679026(A;A) |
Alt | rs200679026(A;A) |
Reference | Rs200679026(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | FBP1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.97367834G>A |
CLNSRC | |
CLNACC | RCV000197614.1, |