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rs2071278

From SNPedia

Orientationminus
Stabilizedminus
Make rs2071278(C;C)
Make rs2071278(C;T)
Make rs2071278(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32197667
GeneNOTCH4
is asnp
is mentioned by
dbSNPrs2071278
ebirs2071278
HLIrs2071278
Exacrs2071278
Varsomers2071278
Maprs2071278
PheGenIrs2071278
hapmaprs2071278
1000 genomesrs2071278
hgdprs2071278
ensemblrs2071278
gopubmedrs2071278
geneviewrs2071278
scholarrs2071278
googlers2071278
pharmgkbrs2071278
gwascentralrs2071278
openSNPrs2071278
23andMers2071278
23andMe allrs2071278
SNP Nexus

SNPshotrs2071278
SNPdbers2071278
MSV3drs2071278
GWAS Ctlgrs2071278
GMAF0.1162
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23028341OA-icon.png]
Trait Complement C3 and C4 levels
Title Genome-wide association study for serum complement C3 and C4 levels in healthy Chinese subjects.
Risk Allele G
P-val 4E-72
Odds Ratio .13 [0.11-0.15] g/L decrease


[PMID 15747258OA-icon.png] A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms.