Tag
Migraine
16 genetic variants with this tag.
| RSID | Gene | Description | Category | ||
|---|---|---|---|---|---|
| rs1003194 | CALCA/CALCB | Intergenic regulatory variant ~26 kb downstream of CALCB (calcitonin gene-rel... | Neurology & Cognition | Strong | |
| rs10166942 | TRPM8 | Upstream regulatory variant of the cold-sensing TRPM8 channel that modulates ... | Neurology & Cognition | Strong | |
| rs10405121 | CACNA1A | Common intronic variant in CACNA1A — the P/Q-type calcium channel gene mutate... | Neurology & Cognition | Strong | |
| rs10456100 | KCNK5 | Intronic variant near KCNK5 that reduces TASK2 potassium channel expression a... | Neurology & Cognition | Strong | |
| rs12598836 | HMOX2 | Intronic variant near heme oxygenase 2 (HMOX2) associated with migraine-with-... | Neurology & Cognition | Moderate | |
| rs2271933 | HCRTR1 Ile408Val | Missense variant in the orexin/hypocretin receptor 1 that alters G-protein si... | Mood & Behavior | Moderate | |
| rs17857135 | RNF213 Met270Thr | Missense variant (Met270Thr) in RNF213, the major moyamoya disease susceptibi... | Neurology & Cognition | Strong | |
| rs2078371 | TSPAN2 | Regulatory variant in the TSPAN2/NGF locus on chromosome 1p13; the C allele i... | Neurology & Cognition | Strong | |
| rs2153535 | BLOC1S5 | Regulatory variant near MUTED/BLOC1S5, a gene whose mouse homolog controls ot... | Neurology & Cognition | Strong | |
| rs2274319 | MEF2D | Intronic variant in MEF2D encoding a key neuronal transcription factor that r... | Neurology & Cognition | Strong | |
| rs56051278 | GPD2 | Intronic variant in GPD2 (mitochondrial glycerol-3-phosphate dehydrogenase), ... | Neurology & Cognition | Strong | |
| rs61734410 | CACNA1H Pro640Leu | Missense variant in CACNA1H encoding the CaV3.2 T-type calcium channel; the L... | Neurology & Cognition | Moderate | |
| rs61759167 | PRDM16 | Intronic PRDM16 variant reaching genome-wide significance in the first motion... | Neurology & Cognition | Strong | |
| rs67338227 | FHL5 | Intronic variant in FHL5 (four and a half LIM domains 5), a transcriptional c... | Neurology & Cognition | Strong | |
| rs6795209 | HTR1F | Intergenic variant at the HTR1F locus on chromosome 3; the minor A allele inc... | Neurology & Cognition | Strong | |
| rs9349379 | PHACTR1 | Intronic regulatory variant in PHACTR1 that controls endothelin-1 and arteria... | Neurology & Cognition | Strong |