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rs1048977

From SNPedia

Orientationplus
Stabilizedplus
Make rs1048977(C;C)
Make rs1048977(C;T)
Make rs1048977(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position20618562
GeneCDA
is asnp
is mentioned by
dbSNPrs1048977
ebirs1048977
HLIrs1048977
Exacrs1048977
Varsomers1048977
Maprs1048977
PheGenIrs1048977
hapmaprs1048977
1000 genomesrs1048977
hgdprs1048977
ensemblrs1048977
gopubmedrs1048977
geneviewrs1048977
scholarrs1048977
googlers1048977
pharmgkbrs1048977
gwascentralrs1048977
openSNPrs1048977
23andMers1048977
23andMe allrs1048977
SNP Nexus

SNPshotrs1048977
SNPdbers1048977
MSV3drs1048977
GWAS Ctlgrs1048977
GMAF0.3145
Max Magnitude


GET Evidence
rs1048977
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.339933
summary



[PMID 26174689] The influence of cytidine deaminase -33delC polymorphism on treatment outcome with high-dose cytarabine in Chinese patients with relapsed acute myeloid leukaemia