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rs8099594

From SNPedia

Orientationplus
Stabilizedplus
Make rs8099594(A;A)
Make rs8099594(A;G)
Make rs8099594(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position49464790
is asnp
is mentioned by
dbSNPrs8099594
ClinGenrs8099594
ebirs8099594
HLIrs8099594
Exacrs8099594
Varsomers8099594
Maprs8099594
PheGenIrs8099594
hapmaprs8099594
1000 genomesrs8099594
hgdprs8099594
ensemblrs8099594
gopubmedrs8099594
geneviewrs8099594
scholarrs8099594
googlers8099594
pharmgkbrs8099594
gwascentralrs8099594
openSNPrs8099594
23andMers8099594
23andMe allrs8099594
SNP Nexus

SNPshotrs8099594
SNPdbers8099594
MSV3drs8099594
GWAS Ctlgrs8099594
GMAF0.4665
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 18391952OA-icon.png]
Trait Height
Title Genome-wide association analysis identifies 20 loci that influence adult height
Risk Allele A
P-val 2.9999999999999999E-7
Odds Ratio 0.05 [0.02-0.08] SD taller - among males


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


[PMID 20846217OA-icon.png] Association of linear growth impairment in pediatric Crohn's disease and a known height locus: a pilot study.


GET Evidence
rs8099594
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.53125
summary