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rs10435604

From SNPedia

Orientationplus
Stabilizedplus
Make rs10435604(C;C)
Make rs10435604(C;T)
Make rs10435604(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position61240115
is asnp
is mentioned by
dbSNPrs10435604
ebirs10435604
HLIrs10435604
Exacrs10435604
Varsomers10435604
Maprs10435604
PheGenIrs10435604
hapmaprs10435604
1000 genomesrs10435604
hgdprs10435604
ensemblrs10435604
gopubmedrs10435604
geneviewrs10435604
scholarrs10435604
googlers10435604
pharmgkbrs10435604
gwascentralrs10435604
openSNPrs10435604
23andMers10435604
23andMe allrs10435604
SNP Nexus

SNPshotrs10435604
SNPdbers10435604
MSV3drs10435604
GWAS Ctlgrs10435604
GMAF0.2934
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs10435604
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.296875
summary