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rs6009824

From SNPedia

Orientationplus
Stabilizedplus
Make rs6009824(A;A)
Make rs6009824(A;G)
Make rs6009824(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position49692725
is asnp
is mentioned by
dbSNPrs6009824
dbSNP (classic)rs6009824
ClinGenrs6009824
ebirs6009824
HLIrs6009824
Exacrs6009824
Gnomadrs6009824
Varsomers6009824
LitVarrs6009824
Maprs6009824
PheGenIrs6009824
Biobankrs6009824
1000 genomesrs6009824
hgdprs6009824
ensemblrs6009824
geneviewrs6009824
scholarrs6009824
googlers6009824
pharmgkbrs6009824
gwascentralrs6009824
openSNPrs6009824
23andMers6009824
SNPshotrs6009824
SNPdbers6009824
MSV3drs6009824
GWAS Ctlgrs6009824
GMAF0.2094
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 21273288OA-icon.png]
Trait
Title Genome-Wide Association Analysis and Fine Mapping of NT-proBNP Level Provide Novel Insight into the Role of the MTHFR-CLCN6-NPPA-NPPB Gene Cluster
Risk Allele A
P-val 0.000007
Odds Ratio 0.1300 [0.07-0.19] unit decrease