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rs16827801

From SNPedia

Orientationplus
Stabilizedplus
Make rs16827801(A;A)
Make rs16827801(A;G)
Make rs16827801(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position231116063
GeneHTR2B, PSMD1
is asnp
is mentioned by
dbSNPrs16827801
ebirs16827801
HLIrs16827801
Exacrs16827801
Varsomers16827801
Maprs16827801
PheGenIrs16827801
hapmaprs16827801
1000 genomesrs16827801
hgdprs16827801
ensemblrs16827801
gopubmedrs16827801
geneviewrs16827801
scholarrs16827801
googlers16827801
pharmgkbrs16827801
gwascentralrs16827801
openSNPrs16827801
23andMers16827801
23andMe allrs16827801
SNP Nexus

SNPshotrs16827801
SNPdbers16827801
MSV3drs16827801
GWAS Ctlgrs16827801
GMAF0.4316
Max Magnitude
? (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