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rs426736

From SNPedia

Orientationminus
Stabilizedminus
Make rs426736(C;C)
Make rs426736(C;T)
Make rs426736(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position196791287
GeneCFHR3
is asnp
is mentioned by
dbSNPrs426736
ebirs426736
HLIrs426736
Exacrs426736
Varsomers426736
Maprs426736
PheGenIrs426736
hapmaprs426736
1000 genomesrs426736
hgdprs426736
ensemblrs426736
gopubmedrs426736
geneviewrs426736
scholarrs426736
googlers426736
pharmgkbrs426736
gwascentralrs426736
openSNPrs426736
23andMers426736
23andMe allrs426736
SNP Nexus

SNPshotrs426736
SNPdbers426736
MSV3drs426736
GWAS Ctlgrs426736
GMAF0.3398
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20694013]
Trait
Title Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease
Risk Allele
P-val 5E-13
Odds Ratio 1.59 [1.41-1.82]
OMIM605336
DescCOMPLEMENT FACTOR H-RELATED 3; CFHR3
Variant
Relatedalso
OMIM134370
Desc
Variant
Relatedalso