rs121913557
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs121913557(A;A) |
Make rs121913557(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 60372202 |
Gene | MC4R |
is a | snp |
is | mentioned by |
dbSNP | rs121913557 |
dbSNP (classic) | rs121913557 |
ClinGen | rs121913557 |
ebi | rs121913557 |
HLI | rs121913557 |
Exac | rs121913557 |
Gnomad | rs121913557 |
Varsome | rs121913557 |
LitVar | rs121913557 |
Map | rs121913557 |
PheGenI | rs121913557 |
Biobank | rs121913557 |
1000 genomes | rs121913557 |
hgdp | rs121913557 |
ensembl | rs121913557 |
geneview | rs121913557 |
scholar | rs121913557 |
rs121913557 | |
pharmgkb | rs121913557 |
gwascentral | rs121913557 |
openSNP | rs121913557 |
23andMe | rs121913557 |
SNPshot | rs121913557 |
SNPdbe | rs121913557 |
MSV3d | rs121913557 |
GWAS Ctlg | rs121913557 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121913557(A;A) |
Alt | rs121913557(A;A) |
Reference | Rs121913557(G;G) |
Significance | Pathogenic |
Disease | Obesity |
Variation | info |
Gene | MC4R |
CLNDBN | Obesity |
Reversed | 1 |
HGVS | NC_000018.9:g.58039435C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000015396.26, |