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rs3122169

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs3122169(A;C)
Make rs3122169(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position55248613
GeneHCRTR2
is asnp
is mentioned by
dbSNPrs3122169
ebirs3122169
HLIrs3122169
Exacrs3122169
Varsomers3122169
Maprs3122169
PheGenIrs3122169
hapmaprs3122169
1000 genomesrs3122169
hgdprs3122169
ensemblrs3122169
gopubmedrs3122169
geneviewrs3122169
scholarrs3122169
googlers3122169
pharmgkbrs3122169
gwascentralrs3122169
openSNPrs3122169
23andMers3122169
23andMe allrs3122169
SNP Nexus

SNPshotrs3122169
SNPdbers3122169
MSV3drs3122169
GWAS Ctlgrs3122169
GMAF0.2631
Max Magnitude0
? (A;A) (A;C) (C;C) 28
OMIM119915
DescCLUSTER HEADACHE, FAMILIAL
Variant
Relatedalso
OMIM602393
DescHYPOCRETIN RECEPTOR 2; HCRTR2
Variant
Relatedalso