rs16827801
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs16827801(A;A) |
Make rs16827801(A;G) |
Make rs16827801(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 231116063 |
Gene | HTR2B, PSMD1 |
is a | snp |
is | mentioned by |
dbSNP | rs16827801 |
dbSNP (classic) | rs16827801 |
ClinGen | rs16827801 |
ebi | rs16827801 |
HLI | rs16827801 |
Exac | rs16827801 |
Gnomad | rs16827801 |
Varsome | rs16827801 |
LitVar | rs16827801 |
Map | rs16827801 |
PheGenI | rs16827801 |
Biobank | rs16827801 |
1000 genomes | rs16827801 |
hgdp | rs16827801 |
ensembl | rs16827801 |
geneview | rs16827801 |
scholar | rs16827801 |
rs16827801 | |
pharmgkb | rs16827801 |
gwascentral | rs16827801 |
openSNP | rs16827801 |
23andMe | rs16827801 |
SNPshot | rs16827801 |
SNPdbe | rs16827801 |
MSV3d | rs16827801 |
GWAS Ctlg | rs16827801 |
GMAF | 0.4316 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19455600] a haplotype consisting of rs16827801(T) and rs10194776(G) associated with increased incidence of migraine without aura among a sample of 528 migraine patients (308 without aura, 220 with aura) and 528 sex-matched migraine-free controls