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rs1895507

From SNPedia

Orientationplus
Stabilizedplus
Make rs1895507(A;A)
Make rs1895507(A;G)
Make rs1895507(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position60428792
is asnp
is mentioned by
dbSNPrs1895507
ebirs1895507
HLIrs1895507
Exacrs1895507
Varsomers1895507
Maprs1895507
PheGenIrs1895507
hapmaprs1895507
1000 genomesrs1895507
hgdprs1895507
ensemblrs1895507
gopubmedrs1895507
geneviewrs1895507
scholarrs1895507
googlers1895507
pharmgkbrs1895507
gwascentralrs1895507
openSNPrs1895507
23andMers1895507
23andMe allrs1895507
SNP Nexus

SNPshotrs1895507
SNPdbers1895507
MSV3drs1895507
GWAS Ctlgrs1895507
GMAF0.2815
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs1895507
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.691667
summary