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rs6782299

From SNPedia

Orientationplus
Stabilizedplus
Make rs6782299(G;G)
Make rs6782299(G;T)
Make rs6782299(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position180832914
GeneLOC101928882
is asnp
is mentioned by
dbSNPrs6782299
ebirs6782299
HLIrs6782299
Exacrs6782299
Varsomers6782299
Maprs6782299
PheGenIrs6782299
hapmaprs6782299
1000 genomesrs6782299
hgdprs6782299
ensemblrs6782299
gopubmedrs6782299
geneviewrs6782299
scholarrs6782299
googlers6782299
pharmgkbrs6782299
gwascentralrs6782299
openSNPrs6782299
23andMers6782299
23andMe allrs6782299
SNP Nexus

SNPshotrs6782299
SNPdbers6782299
MSV3drs6782299
GWAS Ctlgrs6782299
GMAF0.1529
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 19571811OA-icon.png]
Trait Schizophrenia
Title Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
Risk Allele T
P-val 1E-7
Odds Ratio 1.10 None


[PMID 21359210OA-icon.png] Pooled genome-wide analysis to identify novel risk loci for pediatric allergic asthma.


GET Evidence
rs6782299
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.851562
summary