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rs2906966

From SNPedia

Orientationminus
Stabilizedminus
Make rs2906966(A;A)
Make rs2906966(A;C)
Make rs2906966(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position15428200
GeneLOC100287829
is asnp
is mentioned by
dbSNPrs2906966
ebirs2906966
HLIrs2906966
Exacrs2906966
Varsomers2906966
Maprs2906966
PheGenIrs2906966
hapmaprs2906966
1000 genomesrs2906966
hgdprs2906966
ensemblrs2906966
gopubmedrs2906966
geneviewrs2906966
scholarrs2906966
googlers2906966
pharmgkbrs2906966
gwascentralrs2906966
openSNPrs2906966
23andMers2906966
23andMe allrs2906966
SNP Nexus

SNPshotrs2906966
SNPdbers2906966
MSV3drs2906966
GWAS Ctlgrs2906966
GMAF0.1644
Max Magnitude
? (A;A) (A;C) (C;C) 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 0.0000079999999999999996
Odds Ratio NR NR


GET Evidence
rs2906966
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.179688
summary