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rs3917733

From SNPedia

Orientationminus
Stabilizedminus
Make rs3917733(A;A)
Make rs3917733(A;G)
Make rs3917733(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position169611272
GeneSELP
is asnp
is mentioned by
dbSNPrs3917733
ebirs3917733
HLIrs3917733
Exacrs3917733
Varsomers3917733
Maprs3917733
PheGenIrs3917733
hapmaprs3917733
1000 genomesrs3917733
hgdprs3917733
ensemblrs3917733
gopubmedrs3917733
geneviewrs3917733
scholarrs3917733
googlers3917733
pharmgkbrs3917733
gwascentralrs3917733
openSNPrs3917733
23andMers3917733
23andMe allrs3917733
SNP Nexus

SNPshotrs3917733
SNPdbers3917733
MSV3drs3917733
GWAS Ctlgrs3917733
GMAF0.1295
Max Magnitude
Part of a haplotype linked to stroke affecting perhaps 5% of sickle cell anemia patients


[PMID 20401335OA-icon.png] Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.