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rs2079795

From SNPedia

Orientationminus
Stabilizedminus
Make rs2079795(A;A)
Make rs2079795(A;G)
Make rs2079795(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position61419288
is asnp
is mentioned by
dbSNPrs2079795
ebirs2079795
HLIrs2079795
Exacrs2079795
Varsomers2079795
Maprs2079795
PheGenIrs2079795
hapmaprs2079795
1000 genomesrs2079795
hgdprs2079795
ensemblrs2079795
gopubmedrs2079795
geneviewrs2079795
scholarrs2079795
googlers2079795
pharmgkbrs2079795
gwascentralrs2079795
openSNPrs2079795
23andMers2079795
23andMe allrs2079795
SNP Nexus

SNPshotrs2079795
SNPdbers2079795
MSV3drs2079795
GWAS Ctlgrs2079795
GMAF0.3926
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19893584]
Trait Height
Title Identification of 15 loci influencing height in a Korean population
Risk Allele T
P-val 0.000003
Odds Ratio 0.40 [NR] cm increase


[PMID 20027299OA-icon.png] Transferability and fine-mapping of genome-wide associated loci for adult height across human populations.


GET Evidence
rs2079795
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.640625
summary



GWAS snp
PMID [PMID 20881960OA-icon.png]
Trait Height
Title Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Risk Allele T
P-val 2E-24
Odds Ratio .04 [NR] unit increase
GWAS snp
PMID [PMID 23563607OA-icon.png]
Trait Height
Title Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.
Risk Allele T
P-val 1E-18
Odds Ratio 1.20 [NR]