rs121917829
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs121917829(A;A) |
Make rs121917829(A;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 60371489 |
Gene | MC4R |
is a | snp |
is | mentioned by |
dbSNP | rs121917829 |
dbSNP (classic) | rs121917829 |
ClinGen | rs121917829 |
ebi | rs121917829 |
HLI | rs121917829 |
Exac | rs121917829 |
Gnomad | rs121917829 |
Varsome | rs121917829 |
LitVar | rs121917829 |
Map | rs121917829 |
PheGenI | rs121917829 |
Biobank | rs121917829 |
1000 genomes | rs121917829 |
hgdp | rs121917829 |
ensembl | rs121917829 |
geneview | rs121917829 |
scholar | rs121917829 |
rs121917829 | |
pharmgkb | rs121917829 |
gwascentral | rs121917829 |
openSNP | rs121917829 |
23andMe | rs121917829 |
SNPshot | rs121917829 |
SNPdbe | rs121917829 |
MSV3d | rs121917829 |
GWAS Ctlg | rs121917829 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121917829(A;A) |
Alt | rs121917829(A;A) |
Reference | Rs121917829(T;T) |
Significance | Pathogenic |
Disease | Obesity |
Variation | info |
Gene | MC4R |
CLNDBN | Obesity |
Reversed | 1 |
HGVS | NC_000018.9:g.58038722A>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000015408.22, |