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rs6088792

From SNPedia

Orientationplus
Stabilizedplus
Make rs6088792(C;C)
Make rs6088792(C;T)
Make rs6088792(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position35321981
GeneUQCC1
is asnp
is mentioned by
dbSNPrs6088792
ebirs6088792
HLIrs6088792
Exacrs6088792
Varsomers6088792
Maprs6088792
PheGenIrs6088792
hapmaprs6088792
1000 genomesrs6088792
hgdprs6088792
ensemblrs6088792
gopubmedrs6088792
geneviewrs6088792
scholarrs6088792
googlers6088792
pharmgkbrs6088792
gwascentralrs6088792
openSNPrs6088792
23andMers6088792
23andMe allrs6088792
SNP Nexus

SNPshotrs6088792
SNPdbers6088792
MSV3drs6088792
GWAS Ctlgrs6088792
GMAF0.1938
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18391951]
Trait Height
Title Many sequence variants affecting diversity of adult human height
Risk Allele T
P-val 7.9999999999999996E-7
Odds Ratio 4.70 [2.74-6.66] % SD taller


[PMID 20017971OA-icon.png] Assessing the impact of global versus local ancestry in association studies.


GET Evidence
rs6088792
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.21875
summary