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rs986475

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs986475(C;C)
Make rs986475(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31588932
GeneLST1, NCR3
is asnp
is mentioned by
dbSNPrs986475
ebirs986475
HLIrs986475
Exacrs986475
Varsomers986475
Maprs986475
PheGenIrs986475
hapmaprs986475
1000 genomesrs986475
hgdprs986475
ensemblrs986475
gopubmedrs986475
geneviewrs986475
scholarrs986475
googlers986475
pharmgkbrs986475
gwascentralrs986475
openSNPrs986475
23andMers986475
23andMe allrs986475
SNP Nexus

SNPshotrs986475
SNPdbers986475
MSV3drs986475
GWAS Ctlgrs986475
GMAF0.1033
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GET Evidence
rs986475
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0703125
summary