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rs4379368

From SNPedia

Orientationplus
Stabilizedplus
Make rs4379368(C;C)
Make rs4379368(C;T)
Make rs4379368(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position40426601
GeneSUGCT
is asnp
is mentioned by
dbSNPrs4379368
dbSNP (classic)rs4379368
ClinGenrs4379368
ebirs4379368
HLIrs4379368
Exacrs4379368
Gnomadrs4379368
Varsomers4379368
LitVarrs4379368
Maprs4379368
PheGenIrs4379368
Biobankrs4379368
1000 genomesrs4379368
hgdprs4379368
ensemblrs4379368
geneviewrs4379368
scholarrs4379368
googlers4379368
pharmgkbrs4379368
gwascentralrs4379368
openSNPrs4379368
23andMers4379368
SNPshotrs4379368
SNPdbers4379368
MSV3drs4379368
GWAS Ctlgrs4379368
GMAF0.2025
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23793025OA-icon.png]
Trait Migraine
Title Genome-wide meta-analysis identifies new susceptibility loci for migraine.
Risk Allele T
P-val 1E-9
Odds Ratio 1.11 [1.08-1.15]


[PMID 26231841OA-icon.png] Association of genetic loci for migraine susceptibility in the she people of China