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rs7586970

From SNPedia

Orientationplus
Stabilizedplus
Make rs7586970(C;C)
Make rs7586970(C;T)
Make rs7586970(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position187478770
GeneLOC105373786, TFPI
is asnp
is mentioned by
dbSNPrs7586970
dbSNP (classic)rs7586970
ClinGenrs7586970
ebirs7586970
HLIrs7586970
Exacrs7586970
Gnomadrs7586970
Varsomers7586970
LitVarrs7586970
Maprs7586970
PheGenIrs7586970
Biobankrs7586970
1000 genomesrs7586970
hgdprs7586970
ensemblrs7586970
geneviewrs7586970
scholarrs7586970
googlers7586970
pharmgkbrs7586970
gwascentralrs7586970
openSNPrs7586970
23andMers7586970
SNPshotrs7586970
SNPdbers7586970
MSV3drs7586970
GWAS Ctlgrs7586970
GMAF0.2723
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 21378988]
Trait
Title A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease
Risk Allele
P-val 0.000009
Odds Ratio None None


[PMID 20140262OA-icon.png] Maternal and fetal genetic associations of PTGER3 and PON1 with preterm birth.