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rs2040494

From SNPedia

Orientationplus
Stabilizedplus
Make rs2040494(C;C)
Make rs2040494(C;T)
Make rs2040494(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position92627591
GeneCDK6
is asnp
is mentioned by
dbSNPrs2040494
ebirs2040494
HLIrs2040494
Exacrs2040494
Varsomers2040494
Maprs2040494
PheGenIrs2040494
hapmaprs2040494
1000 genomesrs2040494
hgdprs2040494
ensemblrs2040494
gopubmedrs2040494
geneviewrs2040494
scholarrs2040494
googlers2040494
pharmgkbrs2040494
gwascentralrs2040494
openSNPrs2040494
23andMers2040494
23andMe allrs2040494
SNP Nexus

SNPshotrs2040494
SNPdbers2040494
MSV3drs2040494
GWAS Ctlgrs2040494
GMAF0.2883
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18391950OA-icon.png]
Trait Height
Title Identification of ten loci associated with height highlights new biological pathways in human growth
Risk Allele C
P-val 3.9999999999999998E-7
Odds Ratio 0.26 [0.36-0.65] cm shorter
OMIM612223
DescSTATURE QUANTITATIVE TRAIT LOCUS 11; STQTL11
Variant
Relatedalso


GET Evidence
rs2040494
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.632812
summary