rs768720209
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs768720209(A;A) |
Make rs768720209(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 11 |
Position | 126271436 |
Gene | FOXRED1 |
is a | snp |
is | mentioned by |
dbSNP | rs768720209 |
dbSNP (classic) | rs768720209 |
ClinGen | rs768720209 |
ebi | rs768720209 |
HLI | rs768720209 |
Exac | rs768720209 |
Gnomad | rs768720209 |
Varsome | rs768720209 |
LitVar | rs768720209 |
Map | rs768720209 |
PheGenI | rs768720209 |
Biobank | rs768720209 |
1000 genomes | rs768720209 |
hgdp | rs768720209 |
ensembl | rs768720209 |
geneview | rs768720209 |
scholar | rs768720209 |
rs768720209 | |
pharmgkb | rs768720209 |
gwascentral | rs768720209 |
openSNP | rs768720209 |
23andMe | rs768720209 |
SNPshot | rs768720209 |
SNPdbe | rs768720209 |
MSV3d | rs768720209 |
GWAS Ctlg | rs768720209 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs768720209(A;A) |
Alt | rs768720209(A;A) |
Reference | Rs768720209(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | FOXRED1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.126141331G>A |
CLNSRC | |
CLNACC | RCV000196380.1, |