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rs1903364

From SNPedia

Orientationplus
Stabilizedplus
Make rs1903364(C;C)
Make rs1903364(C;T)
Make rs1903364(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position114541108
is asnp
is mentioned by
dbSNPrs1903364
dbSNP (classic)rs1903364
ClinGenrs1903364
ebirs1903364
HLIrs1903364
Exacrs1903364
Gnomadrs1903364
Varsomers1903364
LitVarrs1903364
Maprs1903364
PheGenIrs1903364
Biobankrs1903364
1000 genomesrs1903364
hgdprs1903364
ensemblrs1903364
geneviewrs1903364
scholarrs1903364
googlers1903364
pharmgkbrs1903364
gwascentralrs1903364
openSNPrs1903364
23andMers1903364
SNPshotrs1903364
SNPdbers1903364
MSV3drs1903364
GWAS Ctlgrs1903364
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 23118445OA-icon.png] Comprehensive genomic analyses associate UGT8 variants with musical ability in a Mongolian population.