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rs12735613

From SNPedia

Orientationplus
Stabilizedplus
Make rs12735613(A;A)
Make rs12735613(A;G)
Make rs12735613(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position118341350
is asnp
is mentioned by
dbSNPrs12735613
ebirs12735613
HLIrs12735613
Exacrs12735613
Varsomers12735613
Maprs12735613
PheGenIrs12735613
hapmaprs12735613
1000 genomesrs12735613
hgdprs12735613
ensemblrs12735613
gopubmedrs12735613
geneviewrs12735613
scholarrs12735613
googlers12735613
pharmgkbrs12735613
gwascentralrs12735613
openSNPrs12735613
23andMers12735613
23andMe allrs12735613
SNP Nexus

SNPshotrs12735613
SNPdbers12735613
MSV3drs12735613
GWAS Ctlgrs12735613
GMAF0.2388
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 3.9999999999999998E-11
Odds Ratio 0.08 [0.05-0.11] SD shorter - among males


[PMID 19030899OA-icon.png] Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.


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


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


GET Evidence
rs12735613
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.190476
summary