rs2860174
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2860174(A;A) |
Make rs2860174(A;T) |
Make rs2860174(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 7130707 |
Gene | INSR |
is a | snp |
is | mentioned by |
dbSNP | rs2860174 |
dbSNP (classic) | rs2860174 |
ClinGen | rs2860174 |
ebi | rs2860174 |
HLI | rs2860174 |
Exac | rs2860174 |
Gnomad | rs2860174 |
Varsome | rs2860174 |
LitVar | rs2860174 |
Map | rs2860174 |
PheGenI | rs2860174 |
Biobank | rs2860174 |
1000 genomes | rs2860174 |
hgdp | rs2860174 |
ensembl | rs2860174 |
geneview | rs2860174 |
scholar | rs2860174 |
rs2860174 | |
pharmgkb | rs2860174 |
gwascentral | rs2860174 |
openSNP | rs2860174 |
23andMe | rs2860174 |
SNPshot | rs2860174 |
SNPdbe | rs2860174 |
MSV3d | rs2860174 |
GWAS Ctlg | rs2860174 |
GMAF | 0.186 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
A combined study totaling 1,000+ patients with migraine susceptibility concluded that even larger numbers of individuals are required to exclude or confirm the most likely small effect of rs2860174 on migraine susceptibility.[PMID 18455362]