rs137854505
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs137854505(A;A) |
Make rs137854505(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 136198755 |
Gene | LHX3 |
is a | snp |
is | mentioned by |
dbSNP | rs137854505 |
dbSNP (classic) | rs137854505 |
ClinGen | rs137854505 |
ebi | rs137854505 |
HLI | rs137854505 |
Exac | rs137854505 |
Gnomad | rs137854505 |
Varsome | rs137854505 |
LitVar | rs137854505 |
Map | rs137854505 |
PheGenI | rs137854505 |
Biobank | rs137854505 |
1000 genomes | rs137854505 |
hgdp | rs137854505 |
ensembl | rs137854505 |
geneview | rs137854505 |
scholar | rs137854505 |
rs137854505 | |
pharmgkb | rs137854505 |
gwascentral | rs137854505 |
openSNP | rs137854505 |
23andMe | rs137854505 |
SNPshot | rs137854505 |
SNPdbe | rs137854505 |
MSV3d | rs137854505 |
GWAS Ctlg | rs137854505 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs137854505(A;A) |
Alt | rs137854505(A;A) |
Reference | Rs137854505(G;G) |
Significance | Pathogenic |
Disease | Pituitary hormone deficiency |
Variation | info |
Gene | LHX3 |
CLNDBN | Pituitary hormone deficiency, combined 3 |
Reversed | 1 |
HGVS | NC_000009.11:g.139090601C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000009593.5, |