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rs730532

From SNPedia

Orientationminus
Stabilizedminus
Make rs730532(C;C)
Make rs730532(C;T)
Make rs730532(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position52052093
GeneNID2
is asnp
is mentioned by
dbSNPrs730532
ebirs730532
HLIrs730532
Exacrs730532
Varsomers730532
Maprs730532
PheGenIrs730532
hapmaprs730532
1000 genomesrs730532
hgdprs730532
ensemblrs730532
gopubmedrs730532
geneviewrs730532
scholarrs730532
googlers730532
pharmgkbrs730532
gwascentralrs730532
openSNPrs730532
23andMers730532
23andMe allrs730532
SNP Nexus

SNPshotrs730532
SNPdbers730532
MSV3drs730532
GWAS Ctlgrs730532
GMAF0.3898
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 17903307OA-icon.png]
Trait Other pulmonary function traits
Title Framingham Heart Study genome-wide association: results for pulmonary function measures
Risk Allele
P-val 0.0000060000000000000002
Odds Ratio NR NR


[PMID 17903299OA-icon.png] A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study.


GET Evidence
rs730532
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.609375
summary