rs77485247
From SNPedia
Orientation | plus |
Make rs77485247(A;A) |
Make rs77485247(A;T) |
Make rs77485247(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 18 |
Position | 24460578 |
Gene | HRH4 |
is a | snp |
is | mentioned by |
dbSNP | rs77485247 |
dbSNP (classic) | rs77485247 |
ClinGen | rs77485247 |
ebi | rs77485247 |
HLI | rs77485247 |
Exac | rs77485247 |
Gnomad | rs77485247 |
Varsome | rs77485247 |
LitVar | rs77485247 |
Map | rs77485247 |
PheGenI | rs77485247 |
Biobank | rs77485247 |
1000 genomes | rs77485247 |
hgdp | rs77485247 |
ensembl | rs77485247 |
geneview | rs77485247 |
scholar | rs77485247 |
rs77485247 | |
pharmgkb | rs77485247 |
gwascentral | rs77485247 |
openSNP | rs77485247 |
23andMe | rs77485247 |
SNPshot | rs77485247 |
SNPdbe | rs77485247 |
MSV3d | rs77485247 |
GWAS Ctlg | rs77485247 |
Max Magnitude | 0 |
[PMID 31133025] Histamine H4 receptor gene polymorphisms: a potential contributor to Meniere disease.