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rs1831281

From SNPedia

Orientationminus
Stabilizedminus
Make rs1831281(A;A)
Make rs1831281(A;G)
Make rs1831281(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position196711684
GeneCFH
is asnp
is mentioned by
dbSNPrs1831281
ebirs1831281
HLIrs1831281
Exacrs1831281
Varsomers1831281
Maprs1831281
PheGenIrs1831281
hapmaprs1831281
1000 genomesrs1831281
hgdprs1831281
ensemblrs1831281
gopubmedrs1831281
geneviewrs1831281
scholarrs1831281
googlers1831281
pharmgkbrs1831281
gwascentralrs1831281
openSNPrs1831281
23andMers1831281
23andMe allrs1831281
SNP Nexus

SNPshotrs1831281
SNPdbers1831281
MSV3drs1831281
GWAS Ctlgrs1831281
GMAF0.247
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 21882633] [Influence of genetic mutations on clinical presentation of subretinal neovascularization. Report 1: The impact of CFH and IL-8 genes polymorphism]


[PMID 19861685OA-icon.png] Association of factor H autoantibodies with deletions of CFHR1, CFHR3, CFHR4, and with mutations in CFH, CFI, CD46, and C3 in patients with atypical hemolytic uremic syndrome.