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rs11097397

From SNPedia

Orientationplus
Stabilizedplus
Make rs11097397(G;G)
Make rs11097397(G;T)
Make rs11097397(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position93947701
is asnp
is mentioned by
dbSNPrs11097397
dbSNP (classic)rs11097397
ClinGenrs11097397
ebirs11097397
HLIrs11097397
Exacrs11097397
Gnomadrs11097397
Varsomers11097397
LitVarrs11097397
Maprs11097397
PheGenIrs11097397
Biobankrs11097397
1000 genomesrs11097397
hgdprs11097397
ensemblrs11097397
geneviewrs11097397
scholarrs11097397
googlers11097397
pharmgkbrs11097397
gwascentralrs11097397
openSNPrs11097397
23andMers11097397
SNPshotrs11097397
SNPdbers11097397
MSV3drs11097397
GWAS Ctlgrs11097397
Max Magnitude0
? (G;G) (G;T) (T;T) 28


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