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rs8176592

From SNPedia

Orientationminus
Stabilizedminus
Make rs8176592(C;C)
Make rs8176592(C;T)
Make rs8176592(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position187467965
GeneLOC105373786, TFPI
is asnp
is mentioned by
dbSNPrs8176592
dbSNP (classic)rs8176592
ClinGenrs8176592
ebirs8176592
HLIrs8176592
Exacrs8176592
Gnomadrs8176592
Varsomers8176592
LitVarrs8176592
Maprs8176592
PheGenIrs8176592
Biobankrs8176592
1000 genomesrs8176592
hgdprs8176592
ensemblrs8176592
geneviewrs8176592
scholarrs8176592
googlers8176592
pharmgkbrs8176592
gwascentralrs8176592
openSNPrs8176592
23andMers8176592
SNPshotrs8176592
SNPdbers8176592
MSV3drs8176592
GWAS Ctlgrs8176592
GMAF0.2865
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 23954867] The association of idiopathic recurrent pregnancy loss with polymorphisms in haemostasis-related genes