rs1805094
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs1805094(C;C) |
Make rs1805094(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 65610269 |
Gene | LEPR |
is a | snp |
is | mentioned by |
dbSNP | rs1805094 |
dbSNP (classic) | rs1805094 |
ClinGen | rs1805094 |
ebi | rs1805094 |
HLI | rs1805094 |
Exac | rs1805094 |
Gnomad | rs1805094 |
Varsome | rs1805094 |
LitVar | rs1805094 |
Map | rs1805094 |
PheGenI | rs1805094 |
Biobank | rs1805094 |
1000 genomes | rs1805094 |
hgdp | rs1805094 |
ensembl | rs1805094 |
geneview | rs1805094 |
scholar | rs1805094 |
rs1805094 | |
pharmgkb | rs1805094 |
gwascentral | rs1805094 |
openSNP | rs1805094 |
23andMe | rs1805094 |
SNPshot | rs1805094 |
SNPdbe | rs1805094 |
MSV3d | rs1805094 |
GWAS Ctlg | rs1805094 |
Merged from | Rs8179183 |
GMAF | 0.1446 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
ClinVar | |
---|---|
Risk | rs1805094(C;C) rs1805094(T;T) |
Alt | rs1805094(C;C) rs1805094(T;T) |
Reference | Rs1805094(G;G) |
Significance | Probable-non-pathogenic |
Disease | LEPTIN RECEPTOR POLYMORPHISM Monogenic Non-Syndromic Obesity Leptin receptor deficiency Monogenic diabetes |
Variation | info |
Gene | LEPR LEPROT |
CLNDBN | LEPTIN RECEPTOR POLYMORPHISM Monogenic Non-Syndromic Obesity Leptin receptor deficiency Monogenic diabetes |
Reversed | 0 |
HGVS | NC_000001.10:g.66075952G>C; NC_000001.10:g.66075952G>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000009050.3, RCV000266874.1, RCV000321944.1, RCV000445542.1, |
[PMID 32983895] Combined donor-recipient genotypes of leptin receptor and adiponectin gene polymorphisms affect the incidence of complications after renal transplantation.