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rs3753395

From SNPedia

Orientationplus
Stabilizedplus
Make rs3753395(A;A)
Make rs3753395(A;T)
Make rs3753395(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position196717522
GeneCFH
is asnp
is mentioned by
dbSNPrs3753395
ebirs3753395
HLIrs3753395
Exacrs3753395
Varsomers3753395
Maprs3753395
PheGenIrs3753395
hapmaprs3753395
1000 genomesrs3753395
hgdprs3753395
ensemblrs3753395
gopubmedrs3753395
geneviewrs3753395
scholarrs3753395
googlers3753395
pharmgkbrs3753395
gwascentralrs3753395
openSNPrs3753395
23andMers3753395
23andMe allrs3753395
SNP Nexus

SNPshotrs3753395
SNPdbers3753395
MSV3drs3753395
GWAS Ctlgrs3753395
GMAF0.4582
Max Magnitude
? (A;A) (A;T) (T;T) 28

[PMID 23423485] Genetic variants of complement genes ficolin-2, mannose-binding lectin and complement factor H are associated with leprosy in Han Chinese from Southwest China


[PMID 16936733OA-icon.png] CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration.


[PMID 25612476] Investigating the CFH Gene Polymorphisms as a Risk Factor for Age-related Macular Degeneration in an Iranian Population