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rs62187992

From SNPedia

Orientationplus
Stabilizedplus
Make rs62187992(A;A)
Make rs62187992(A;G)
Make rs62187992(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position212677971
is asnp
is mentioned by
dbSNPrs62187992
dbSNP (old)rs62187992
ClinGenrs62187992
ebirs62187992
HLIrs62187992
Exacrs62187992
Gnomadrs62187992
Varsomers62187992
Maprs62187992
PheGenIrs62187992
Biobankrs62187992
1000 genomesrs62187992
hgdprs62187992
ensemblrs62187992
gopubmedrs62187992
geneviewrs62187992
scholarrs62187992
googlers62187992
pharmgkbrs62187992
gwascentralrs62187992
openSNPrs62187992
23andMers62187992
23andMe allrs62187992
SNP Nexus

SNPshotrs62187992
SNPdbers62187992
MSV3drs62187992
GWAS Ctlgrs62187992
Max Magnitude

[PMID 27490645] Genetic variation 25.1 Mb upstream of tissue factor pathway inhibitor is associated with TFPI plasma levels and venous thromboembolism.