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rs1856801

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1856801(A;A)
Make rs1856801(A;C)
ReferenceGRCh38 38.1/142
Chromosome10
Position110632404
is asnp
is mentioned by
dbSNPrs1856801
ebirs1856801
HLIrs1856801
Exacrs1856801
Varsomers1856801
Maprs1856801
PheGenIrs1856801
hapmaprs1856801
1000 genomesrs1856801
hgdprs1856801
ensemblrs1856801
gopubmedrs1856801
geneviewrs1856801
scholarrs1856801
googlers1856801
pharmgkbrs1856801
gwascentralrs1856801
openSNPrs1856801
23andMers1856801
23andMe allrs1856801
SNP Nexus

SNPshotrs1856801
SNPdbers1856801
MSV3drs1856801
GWAS Ctlgrs1856801
GMAF0.14
Max Magnitude0
? (A;A) (A;C) (C;C) 28


GET Evidence
rs1856801
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.164062
summary