rs786204663
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs786204663(-;-) |
Make rs786204663(-;C) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 5 |
Position | 177994138 |
Gene | PROP1 |
is a | snp |
is | mentioned by |
dbSNP | rs786204663 |
dbSNP (classic) | rs786204663 |
ClinGen | rs786204663 |
ebi | rs786204663 |
HLI | rs786204663 |
Exac | rs786204663 |
Gnomad | rs786204663 |
Varsome | rs786204663 |
LitVar | rs786204663 |
Map | rs786204663 |
PheGenI | rs786204663 |
Biobank | rs786204663 |
1000 genomes | rs786204663 |
hgdp | rs786204663 |
ensembl | rs786204663 |
geneview | rs786204663 |
scholar | rs786204663 |
rs786204663 | |
pharmgkb | rs786204663 |
gwascentral | rs786204663 |
openSNP | rs786204663 |
23andMe | rs786204663 |
SNPshot | rs786204663 |
SNPdbe | rs786204663 |
MSV3d | rs786204663 |
GWAS Ctlg | rs786204663 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786204663(-;-) |
Alt | rs786204663(-;-) |
Reference | Rs786204663(C;C) |
Significance | Probable-Pathogenic |
Disease | Pituitary hormone deficiency |
Variation | info |
Gene | PROP1 |
CLNDBN | Pituitary hormone deficiency, combined 2 |
Reversed | 1 |
HGVS | NC_000005.9:g.177421139delG |
CLNSRC | |
CLNACC | RCV000169459.1, |