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rs6724465

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs6724465(A;A)
Make rs6724465(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position219079124
GeneNHEJ1
is asnp
is mentioned by
dbSNPrs6724465
ebirs6724465
HLIrs6724465
Exacrs6724465
Varsomers6724465
Maprs6724465
PheGenIrs6724465
hapmaprs6724465
1000 genomesrs6724465
hgdprs6724465
ensemblrs6724465
gopubmedrs6724465
geneviewrs6724465
scholarrs6724465
googlers6724465
pharmgkbrs6724465
gwascentralrs6724465
openSNPrs6724465
23andMers6724465
23andMe allrs6724465
SNP Nexus

SNPshotrs6724465
SNPdbers6724465
MSV3drs6724465
GWAS Ctlgrs6724465
GMAF0.1111
Max Magnitude0
? (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 2E-8
Odds Ratio 0.06 [0.02-0.10] SD shorter - among males


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


[PMID 19039035OA-icon.png] Genome-wide association study identifies two novel loci containing FLNB and SBF2 genes underlying stature variation.


[PMID 19481195OA-icon.png] The primordial growth disorder 3-M syndrome connects ubiquitination to the cytoskeletal adaptor OBSL1.


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


GET Evidence
rs6724465
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.117188
summary