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rs4905865

From SNPedia

Orientationplus
Stabilizedplus
Make rs4905865(G;G)
Make rs4905865(G;T)
Make rs4905865(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position99609722
GeneFAM193A
is asnp
is mentioned by
dbSNPrs4905865
ebirs4905865
HLIrs4905865
Exacrs4905865
Varsomers4905865
Maprs4905865
PheGenIrs4905865
hapmaprs4905865
1000 genomesrs4905865
hgdprs4905865
ensemblrs4905865
gopubmedrs4905865
geneviewrs4905865
scholarrs4905865
googlers4905865
pharmgkbrs4905865
gwascentralrs4905865
openSNPrs4905865
23andMers4905865
23andMe allrs4905865
SNP Nexus

SNPshotrs4905865
SNPdbers4905865
MSV3drs4905865
GWAS Ctlgrs4905865
GMAF0.3802
Max Magnitude
? (G;G) (G;T) (T;T) 28


GET Evidence
rs4905865
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.626984
summary