rs147564881
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs147564881(C;C) |
Make rs147564881(C;G) |
Make rs147564881(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 3 |
Position | 155118765 |
Gene | MME |
is a | snp |
is | mentioned by |
dbSNP | rs147564881 |
dbSNP (classic) | rs147564881 |
ClinGen | rs147564881 |
ebi | rs147564881 |
HLI | rs147564881 |
Exac | rs147564881 |
Gnomad | rs147564881 |
Varsome | rs147564881 |
LitVar | rs147564881 |
Map | rs147564881 |
PheGenI | rs147564881 |
Biobank | rs147564881 |
1000 genomes | rs147564881 |
hgdp | rs147564881 |
ensembl | rs147564881 |
geneview | rs147564881 |
scholar | rs147564881 |
rs147564881 | |
pharmgkb | rs147564881 |
gwascentral | rs147564881 |
openSNP | rs147564881 |
23andMe | rs147564881 |
SNPshot | rs147564881 |
SNPdbe | rs147564881 |
MSV3d | rs147564881 |
GWAS Ctlg | rs147564881 |
Max Magnitude | 0 |
[PMID 28831700] Screening of genetic variants in ADCYAP1R1, MME and 14q21 in a Swedish cluster headache cohort.