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rs16840639

From SNPedia

Orientationplus
Stabilizedplus
Make rs16840639(C;C)
Make rs16840639(C;T)
Make rs16840639(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position196855643
GeneLOC100289145
is asnp
is mentioned by
dbSNPrs16840639
ebirs16840639
HLIrs16840639
Exacrs16840639
Varsomers16840639
Maprs16840639
PheGenIrs16840639
hapmaprs16840639
1000 genomesrs16840639
hgdprs16840639
ensemblrs16840639
gopubmedrs16840639
geneviewrs16840639
scholarrs16840639
googlers16840639
pharmgkbrs16840639
gwascentralrs16840639
openSNPrs16840639
23andMers16840639
23andMe allrs16840639
SNP Nexus

SNPshotrs16840639
SNPdbers16840639
MSV3drs16840639
GWAS Ctlgrs16840639
GMAF0.1887
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19789632OA-icon.png] We found that YRI have significantly lower copy number of CFHR3 gene (Complement Factor H-Related gene 3) than CEU and ASN individuals. In addition, we have observed that this variant is well tagged by a SNP (rs16840639; r2 = 0.79)


[PMID 21637784OA-icon.png] Association of genetic variants in complement factor h and factor h-related genes with systemic lupus erythematosus susceptibility


[PMID 23582991] Genetic Influences on the Outcome of Anti-Vascular Endothelial Growth Factor Treatment in Neovascular Age-related Macular Degeneration