rs776720591
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs776720591(A;G) |
Make rs776720591(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 22 |
Position | 37755099 |
Gene | TRIOBP |
is a | snp |
is | mentioned by |
dbSNP | rs776720591 |
dbSNP (classic) | rs776720591 |
ClinGen | rs776720591 |
ebi | rs776720591 |
HLI | rs776720591 |
Exac | rs776720591 |
Gnomad | rs776720591 |
Varsome | rs776720591 |
LitVar | rs776720591 |
Map | rs776720591 |
PheGenI | rs776720591 |
Biobank | rs776720591 |
1000 genomes | rs776720591 |
hgdp | rs776720591 |
ensembl | rs776720591 |
geneview | rs776720591 |
scholar | rs776720591 |
rs776720591 | |
pharmgkb | rs776720591 |
gwascentral | rs776720591 |
openSNP | rs776720591 |
23andMe | rs776720591 |
SNPshot | rs776720591 |
SNPdbe | rs776720591 |
MSV3d | rs776720591 |
GWAS Ctlg | rs776720591 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs776720591(G;G) |
Alt | rs776720591(G;G) |
Reference | Rs776720591(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | TRIOBP |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000022.10:g.38151106A>G |
CLNSRC | |
CLNACC | RCV000480502.1, |