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rs727979

From SNPedia

Orientationminus
Stabilizedminus
Make rs727979(A;A)
Make rs727979(A;G)
Make rs727979(G;G)
ReferenceGRCh38 38.1/142
Chromosome6
Position149272784
GeneTAB2
is asnp
is mentioned by
dbSNPrs727979
ebirs727979
HLIrs727979
Exacrs727979
Varsomers727979
Maprs727979
PheGenIrs727979
hapmaprs727979
1000 genomesrs727979
hgdprs727979
ensemblrs727979
gopubmedrs727979
geneviewrs727979
scholarrs727979
googlers727979
pharmgkbrs727979
gwascentralrs727979
openSNPrs727979
23andMers727979
23andMe allrs727979
SNP Nexus

SNPshotrs727979
SNPdbers727979
MSV3drs727979
GWAS Ctlgrs727979
GMAF0.1928
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 17903294OA-icon.png]
Trait Hemostatic factors and hematological phenotypes
Title Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study
Risk Allele
P-val 0.0000079999999999999996
Odds Ratio NR NR


GET Evidence
rs727979
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.132812
summary