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rs4715291

From SNPedia

Orientationplus
Make rs4715291(C;C)
Make rs4715291(C;T)
Make rs4715291(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position52248562
is asnp
is mentioned by
dbSNPrs4715291
ebirs4715291
HLIrs4715291
Exacrs4715291
Varsomers4715291
Maprs4715291
PheGenIrs4715291
hapmaprs4715291
1000 genomesrs4715291
hgdprs4715291
ensemblrs4715291
gopubmedrs4715291
geneviewrs4715291
scholarrs4715291
googlers4715291
pharmgkbrs4715291
gwascentralrs4715291
openSNPrs4715291
23andMers4715291
23andMe allrs4715291
SNP Nexus

SNPshotrs4715291
SNPdbers4715291
MSV3drs4715291
GWAS Ctlgrs4715291
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 26667835] IL17F and IL17RA genetic variants increase risk of cerebral malaria in two African populations.