Have questions? Visit https://www.reddit.com/r/SNPedia

rs6581612

From SNPedia

Orientationplus
Stabilizedplus
Make rs6581612(A;A)
Make rs6581612(A;C)
Make rs6581612(C;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position65140844
is asnp
is mentioned by
dbSNPrs6581612
ebirs6581612
HLIrs6581612
Exacrs6581612
Varsomers6581612
Maprs6581612
PheGenIrs6581612
hapmaprs6581612
1000 genomesrs6581612
hgdprs6581612
ensemblrs6581612
gopubmedrs6581612
geneviewrs6581612
scholarrs6581612
googlers6581612
pharmgkbrs6581612
gwascentralrs6581612
openSNPrs6581612
23andMers6581612
23andMe allrs6581612
SNP Nexus

SNPshotrs6581612
SNPdbers6581612
MSV3drs6581612
GWAS Ctlgrs6581612
GMAF0.2213
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 22504421OA-icon.png]
Trait
Title Common variants at 12q14 and 12q24 are associated with hippocampal volume.
Risk Allele C
P-val 7E-11
Odds Ratio 63.3000 None


GET Evidence
rs6581612
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.726562
summary



[PMID 23315860] Genetic variations in the Wnt signaling pathway affect lung function in asthma patients