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rs9395066

From SNPedia

Orientationplus
Stabilizedplus
Make rs9395066(A;A)
Make rs9395066(A;C)
Make rs9395066(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position45127426
GeneSUPT3H
is asnp
is mentioned by
dbSNPrs9395066
ebirs9395066
HLIrs9395066
Exacrs9395066
Varsomers9395066
Maprs9395066
PheGenIrs9395066
hapmaprs9395066
1000 genomesrs9395066
hgdprs9395066
ensemblrs9395066
gopubmedrs9395066
geneviewrs9395066
scholarrs9395066
googlers9395066
pharmgkbrs9395066
gwascentralrs9395066
openSNPrs9395066
23andMers9395066
23andMe allrs9395066
SNP Nexus

SNPshotrs9395066
SNPdbers9395066
MSV3drs9395066
GWAS Ctlgrs9395066
GMAF0.4568
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 18391951]
Trait Height
Title Many sequence variants affecting diversity of adult human height
Risk Allele C
P-val 0.0000079999999999999996
Odds Ratio 3.50 [1.93-5.07] % SD taller


GET Evidence
rs9395066
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.398438
summary