rs751160202
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs751160202(A;G) |
Make rs751160202(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 18 |
Position | 60372144 |
Gene | MC4R |
is a | snp |
is | mentioned by |
dbSNP | rs751160202 |
dbSNP (classic) | rs751160202 |
ClinGen | rs751160202 |
ebi | rs751160202 |
HLI | rs751160202 |
Exac | rs751160202 |
Gnomad | rs751160202 |
Varsome | rs751160202 |
LitVar | rs751160202 |
Map | rs751160202 |
PheGenI | rs751160202 |
Biobank | rs751160202 |
1000 genomes | rs751160202 |
hgdp | rs751160202 |
ensembl | rs751160202 |
geneview | rs751160202 |
scholar | rs751160202 |
rs751160202 | |
pharmgkb | rs751160202 |
gwascentral | rs751160202 |
openSNP | rs751160202 |
23andMe | rs751160202 |
SNPshot | rs751160202 |
SNPdbe | rs751160202 |
MSV3d | rs751160202 |
GWAS Ctlg | rs751160202 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs751160202(C;C) rs751160202(G;G) |
Alt | rs751160202(C;C) rs751160202(G;G) |
Reference | Rs751160202(A;A) |
Significance | Pathogenic |
Disease | Obesity |
Variation | info |
Gene | MC4R |
CLNDBN | Obesity, autosomal dominant |
Reversed | 0 |
HGVS | NC_000018.9:g.58039377A>C |
CLNSRC | |
CLNACC | RCV000194758.1, |