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rs11684454

From SNPedia

Orientationplus
Stabilizedplus
Make rs11684454(A;A)
Make rs11684454(A;G)
Make rs11684454(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position118005492
GeneCCDC93
is asnp
is mentioned by
dbSNPrs11684454
ebirs11684454
HLIrs11684454
Exacrs11684454
Varsomers11684454
Maprs11684454
PheGenIrs11684454
hapmaprs11684454
1000 genomesrs11684454
hgdprs11684454
ensemblrs11684454
gopubmedrs11684454
geneviewrs11684454
scholarrs11684454
googlers11684454
pharmgkbrs11684454
gwascentralrs11684454
openSNPrs11684454
23andMers11684454
23andMe allrs11684454
SNP Nexus

SNPshotrs11684454
SNPdbers11684454
MSV3drs11684454
GWAS Ctlgrs11684454
GMAF0.3012
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs11684454
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.304688
summary