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rs3136516

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs3136516(A;A)
Make rs3136516(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position46739206
GeneF2
is asnp
is mentioned by
dbSNPrs3136516
ebirs3136516
HLIrs3136516
Exacrs3136516
Varsomers3136516
Maprs3136516
PheGenIrs3136516
hapmaprs3136516
1000 genomesrs3136516
hgdprs3136516
ensemblrs3136516
gopubmedrs3136516
geneviewrs3136516
scholarrs3136516
googlers3136516
pharmgkbrs3136516
gwascentralrs3136516
openSNPrs3136516
23andMers3136516
23andMe allrs3136516
SNP Nexus

SNPshotrs3136516
SNPdbers3136516
MSV3drs3136516
GWAS Ctlgrs3136516
GMAF0.3058
Max Magnitude0
? (A;A) (A;G) (G;G) 28

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


[PMID 24226152] Influence of single nucleotide polymorphisms on thrombin generation in factor V Leiden heterozygotes


[PMID 21239755OA-icon.png] Functional polymorphisms of the coagulation factor II gene (F2) and susceptibility to systemic lupus erythematosus.


ClinVar
Risk rs3136516(A;A)
Alt rs3136516(A;A)
Reference rs3136516(G;G)
Significance Unknown
Disease Thrombophilia
Variation info
Gene F2
CLNDBN Thrombophilia
Reversed 0
HGVS NC_000011.9:g.46760756G>A
CLNSRC
CLNACC RCV000133511.2,