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rs3917862

From SNPedia

Orientationminus
Make rs3917862(C;C)
Make rs3917862(C;T)
Make rs3917862(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position169623875
GeneSELP
is asnp
is mentioned by
dbSNPrs3917862
ebirs3917862
HLIrs3917862
Exacrs3917862
Varsomers3917862
Maprs3917862
PheGenIrs3917862
hapmaprs3917862
1000 genomesrs3917862
hgdprs3917862
ensemblrs3917862
gopubmedrs3917862
geneviewrs3917862
scholarrs3917862
googlers3917862
pharmgkbrs3917862
gwascentralrs3917862
openSNPrs3917862
23andMers3917862
23andMe allrs3917862
SNP Nexus

SNPshotrs3917862
SNPdbers3917862
MSV3drs3917862
GWAS Ctlgrs3917862
Max Magnitude
? (C;C) (C;T) (T;T) 28
Neanderthal [PMID 26912863]