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rs1006798

From SNPedia

Orientationplus
Stabilizedplus
Make rs1006798(A;A)
Make rs1006798(A;G)
Make rs1006798(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position3256646
GeneMSANTD1
is asnp
is mentioned by
dbSNPrs1006798
ClinGenrs1006798
ebirs1006798
HLIrs1006798
Exacrs1006798
Varsomers1006798
Maprs1006798
PheGenIrs1006798
hapmaprs1006798
1000 genomesrs1006798
hgdprs1006798
ensemblrs1006798
gopubmedrs1006798
geneviewrs1006798
scholarrs1006798
googlers1006798
pharmgkbrs1006798
gwascentralrs1006798
openSNPrs1006798
23andMers1006798
23andMe allrs1006798
SNP Nexus

SNPshotrs1006798
SNPdbers1006798
MSV3drs1006798
GWAS Ctlgrs1006798
GMAF0.3168
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs1006798
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.28125
summary