rs1893220
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1893220(A;A) |
Make rs1893220(A;C) |
Make rs1893220(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 13916295 |
Gene | MC2R |
is a | snp |
is | mentioned by |
dbSNP | rs1893220 |
dbSNP (classic) | rs1893220 |
ClinGen | rs1893220 |
ebi | rs1893220 |
HLI | rs1893220 |
Exac | rs1893220 |
Gnomad | rs1893220 |
Varsome | rs1893220 |
LitVar | rs1893220 |
Map | rs1893220 |
PheGenI | rs1893220 |
Biobank | rs1893220 |
1000 genomes | rs1893220 |
hgdp | rs1893220 |
ensembl | rs1893220 |
geneview | rs1893220 |
scholar | rs1893220 |
rs1893220 | |
pharmgkb | rs1893220 |
gwascentral | rs1893220 |
openSNP | rs1893220 |
23andMe | rs1893220 |
SNPshot | rs1893220 |
SNPdbe | rs1893220 |
MSV3d | rs1893220 |
GWAS Ctlg | rs1893220 |
GMAF | 0.3108 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 19024088] rs1893220 and rs2186944 efficacy of ACTH therapy on infantile spasms.
[PMID 20042918] ACTH receptor (MC2R) promoter variants associated with infantile spasms modulate MC2R expression and responsiveness to ACTH
[PMID 26115626] Association between two promoter polymorphisms (rs1893219 and rs1893220) of MC2R gene and intracerebral hemorrhage in Korean population