rs6019

minus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs6019(C;C)

Make rs6019(C;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

169572275

Gene

F5

is a	snp
is	mentioned by
dbSNP	rs6019
dbSNP (classic)	rs6019
ClinGen	rs6019
ebi	rs6019
HLI	rs6019
Exac	rs6019
Gnomad	rs6019
Varsome	rs6019
LitVar	rs6019
Map	rs6019
PheGenI	rs6019
Biobank	rs6019
1000 genomes	rs6019
hgdp	rs6019
ensembl	rs6019
geneview	rs6019
scholar	rs6019
google	rs6019
pharmgkb	rs6019
gwascentral	rs6019
openSNP	rs6019
23andMe	rs6019
SNPshot	rs6019
SNPdbe	rs6019
MSV3d	rs6019
GWAS Ctlg	rs6019

GMAF

0.1084

Max Magnitude

0

?

(C;C) (C;G) (G;G)

28

[PMID 19020903 ] rs6019 and rs6022 maternal smoking on PTD and gestational age. Compared with non-smoking mothers carrying rs6019(C) associated with significantly increased risk of PTD (OR(95% CI): 2.1(1.2-3.6) for GC; 5.7(2.1-15.0) for CC; p-interaction = 0.02

[PMID 22281051 ] Association of Factor V Gene Polymorphism With Arteriovenous Graft Failure

[PMID 16642433 ] Polymorphism in maternal LRP8 gene is associated with fetal growth.

ClinVar
Risk	rs6019(C;C)
Alt	rs6019(C;C)
Reference	Rs6019(G;G)
Significance	Probable-non-pathogenic
Disease	not specified Thrombophilia Thrombophilia due to activated protein C resistance Factor V deficiency Budd-Chiari syndrome
Variation	info
Gene	F5
CLNDBN	not specified Thrombophilia Thrombophilia due to activated protein C resistance Factor V deficiency Budd-Chiari syndrome
Reversed	1
HGVS	NC_000001.10:g.169541513C>G
CLNSRC
CLNACC	RCV000242383.1, RCV000275358.1, RCV000315209.1, RCV000369930.1, RCV000400869.1,