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rs340669

From SNPedia

Orientationminus
Stabilizedplus
Make rs340669(A;A)
Make rs340669(A;G)
Make rs340669(G;G)
ReferenceGRCh38 38.1/142
Chromosome5
Position8438418
GeneSNORD19B
is asnp
is mentioned by
dbSNPrs340669
ebirs340669
HLIrs340669
Exacrs340669
Varsomers340669
Maprs340669
PheGenIrs340669
hapmaprs340669
1000 genomesrs340669
hgdprs340669
ensemblrs340669
gopubmedrs340669
geneviewrs340669
scholarrs340669
googlers340669
pharmgkbrs340669
gwascentralrs340669
openSNPrs340669
23andMers340669
23andMe allrs340669
SNP Nexus

SNPshotrs340669
SNPdbers340669
MSV3drs340669
GWAS Ctlgrs340669
GMAF0.3278
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs340669
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.601562
summary