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rs999986

From SNPedia

Orientationminus
Stabilizedplus
Make rs999986(G;G)
Make rs999986(G;T)
Make rs999986(T;T)
ReferenceGRCh38 38.1/142
Chromosome14
Position95337519
is asnp
is mentioned by
dbSNPrs999986
ebirs999986
HLIrs999986
Exacrs999986
Varsomers999986
Maprs999986
PheGenIrs999986
hapmaprs999986
1000 genomesrs999986
hgdprs999986
ensemblrs999986
gopubmedrs999986
geneviewrs999986
scholarrs999986
googlers999986
pharmgkbrs999986
gwascentralrs999986
openSNPrs999986
23andMers999986
23andMe allrs999986
SNP Nexus

SNPshotrs999986
SNPdbers999986
MSV3drs999986
GWAS Ctlgrs999986
GMAF0.3062
Max Magnitude
? (G;G) (G;T) (T;T) 28


GET Evidence
rs999986
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.210938
summary