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rs6088813

From SNPedia

Orientationplus
Stabilizedplus
Make rs6088813(A;A)
Make rs6088813(A;C)
Make rs6088813(C;C)
ReferenceGRCh38 38.1/141
Chromosome20
Position35387378
GeneUQCC1
is asnp
is mentioned by
dbSNPrs6088813
ebirs6088813
HLIrs6088813
Exacrs6088813
Varsomers6088813
Maprs6088813
PheGenIrs6088813
hapmaprs6088813
1000 genomesrs6088813
hgdprs6088813
ensemblrs6088813
gopubmedrs6088813
geneviewrs6088813
scholarrs6088813
googlers6088813
pharmgkbrs6088813
gwascentralrs6088813
openSNPrs6088813
23andMers6088813
23andMe allrs6088813
SNP Nexus

SNPshotrs6088813
SNPdbers6088813
MSV3drs6088813
GWAS Ctlgrs6088813
GMAF0.4073
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 19343178OA-icon.png]
Trait Height
Title Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size
Risk Allele
P-val 1E-13
Odds Ratio
OMIM612228
DescSTATURE QUANTITATIVE TRAIT LOCUS 14; STQTL14
Variant
Relatedalso



GET Evidence
rs6088813
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.5
summary