rs747681609
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs747681609(C;T) |
Make rs747681609(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 18 |
Position | 60371856 |
Gene | MC4R |
is a | snp |
is | mentioned by |
dbSNP | rs747681609 |
dbSNP (classic) | rs747681609 |
ClinGen | rs747681609 |
ebi | rs747681609 |
HLI | rs747681609 |
Exac | rs747681609 |
Gnomad | rs747681609 |
Varsome | rs747681609 |
LitVar | rs747681609 |
Map | rs747681609 |
PheGenI | rs747681609 |
Biobank | rs747681609 |
1000 genomes | rs747681609 |
hgdp | rs747681609 |
ensembl | rs747681609 |
geneview | rs747681609 |
scholar | rs747681609 |
rs747681609 | |
pharmgkb | rs747681609 |
gwascentral | rs747681609 |
openSNP | rs747681609 |
23andMe | rs747681609 |
SNPshot | rs747681609 |
SNPdbe | rs747681609 |
MSV3d | rs747681609 |
GWAS Ctlg | rs747681609 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs747681609(T;T) |
Alt | rs747681609(T;T) |
Reference | Rs747681609(C;C) |
Significance | Probable-Pathogenic |
Disease | Obesity |
Variation | info |
Gene | MC4R |
CLNDBN | Obesity |
Reversed | 0 |
HGVS | NC_000018.9:g.58039089C>T |
CLNSRC | Illumina |
CLNACC | RCV000332082.1, |