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rs10194776

From SNPedia

Orientationplus
Stabilizedplus
Make rs10194776(C;C)
Make rs10194776(C;T)
Make rs10194776(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position231115305
GeneHTR2B, PSMD1
is asnp
is mentioned by
dbSNPrs10194776
ebirs10194776
HLIrs10194776
Exacrs10194776
Varsomers10194776
Maprs10194776
PheGenIrs10194776
hapmaprs10194776
1000 genomesrs10194776
hgdprs10194776
ensemblrs10194776
gopubmedrs10194776
geneviewrs10194776
scholarrs10194776
googlers10194776
pharmgkbrs10194776
gwascentralrs10194776
openSNPrs10194776
23andMers10194776
23andMe allrs10194776
SNP Nexus

SNPshotrs10194776
SNPdbers10194776
MSV3drs10194776
GWAS Ctlgrs10194776
GMAF0.4261
Max Magnitude
? (C;C) (C;T) (T;T) 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


[PMID 23774082] No Association between a polymorphism in the serotonin receptor 2B (HTR2B) gene and personality traits in healthy Japanese subjects.