rs376239580
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs376239580(A;A) |
Make rs376239580(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 20 |
Position | 5302632 |
Gene | PROKR2 |
is a | snp |
is | mentioned by |
dbSNP | rs376239580 |
dbSNP (classic) | rs376239580 |
ClinGen | rs376239580 |
ebi | rs376239580 |
HLI | rs376239580 |
Exac | rs376239580 |
Gnomad | rs376239580 |
Varsome | rs376239580 |
LitVar | rs376239580 |
Map | rs376239580 |
PheGenI | rs376239580 |
Biobank | rs376239580 |
1000 genomes | rs376239580 |
hgdp | rs376239580 |
ensembl | rs376239580 |
geneview | rs376239580 |
scholar | rs376239580 |
rs376239580 | |
pharmgkb | rs376239580 |
gwascentral | rs376239580 |
openSNP | rs376239580 |
23andMe | rs376239580 |
SNPshot | rs376239580 |
SNPdbe | rs376239580 |
MSV3d | rs376239580 |
GWAS Ctlg | rs376239580 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs376239580(A;A) |
Alt | rs376239580(A;A) |
Reference | Rs376239580(G;G) |
Significance | Probable-Pathogenic |
Disease | Hypogonadotrophic hypogonadism |
Variation | info |
Gene | PROKR2 |
CLNDBN | Hypogonadotrophic hypogonadism |
Reversed | 0 |
HGVS | NC_000020.10:g.5283278G>A |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000156965.1, |