rs772213710
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs772213710(C;T) |
Make rs772213710(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 18 |
Position | 60372069 |
Gene | MC4R |
is a | snp |
is | mentioned by |
dbSNP | rs772213710 |
dbSNP (classic) | rs772213710 |
ClinGen | rs772213710 |
ebi | rs772213710 |
HLI | rs772213710 |
Exac | rs772213710 |
Gnomad | rs772213710 |
Varsome | rs772213710 |
LitVar | rs772213710 |
Map | rs772213710 |
PheGenI | rs772213710 |
Biobank | rs772213710 |
1000 genomes | rs772213710 |
hgdp | rs772213710 |
ensembl | rs772213710 |
geneview | rs772213710 |
scholar | rs772213710 |
rs772213710 | |
pharmgkb | rs772213710 |
gwascentral | rs772213710 |
openSNP | rs772213710 |
23andMe | rs772213710 |
SNPshot | rs772213710 |
SNPdbe | rs772213710 |
MSV3d | rs772213710 |
GWAS Ctlg | rs772213710 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs772213710(T;T) |
Alt | rs772213710(T;T) |
Reference | Rs772213710(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | MC4R |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000018.9:g.58039302C>T |
CLNSRC | |
CLNACC | RCV000432683.1, |