Have questions? Visit https://www.reddit.com/r/SNPedia

rs1312895

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs1312895(A;A)
Make rs1312895(A;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position118667800
is asnp
is mentioned by
dbSNPrs1312895
ebirs1312895
HLIrs1312895
Exacrs1312895
Varsomers1312895
Maprs1312895
PheGenIrs1312895
hapmaprs1312895
1000 genomesrs1312895
hgdprs1312895
ensemblrs1312895
gopubmedrs1312895
geneviewrs1312895
scholarrs1312895
googlers1312895
pharmgkbrs1312895
gwascentralrs1312895
openSNPrs1312895
23andMers1312895
23andMe allrs1312895
SNP Nexus

SNPshotrs1312895
SNPdbers1312895
MSV3drs1312895
GWAS Ctlgrs1312895
GMAF0.2029
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GET Evidence
rs1312895
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.804688
summary