rs6022

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs6022(G;T)

Make rs6022(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

169560588

Gene

F5

is a	snp
is	mentioned by
dbSNP	rs6022
dbSNP (classic)	rs6022
ClinGen	rs6022
ebi	rs6022
HLI	rs6022
Exac	rs6022
Gnomad	rs6022
Varsome	rs6022
LitVar	rs6022
Map	rs6022
PheGenI	rs6022
Biobank	rs6022
1000 genomes	rs6022
hgdp	rs6022
ensembl	rs6022
geneview	rs6022
scholar	rs6022
google	rs6022
pharmgkb	rs6022
gwascentral	rs6022
openSNP	rs6022
23andMe	rs6022
SNPshot	rs6022
SNPdbe	rs6022
MSV3d	rs6022
GWAS Ctlg	rs6022

GMAF

0.4132

Max Magnitude

0

?

(G;G) (G;T) (T;T)

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

ClinVar
Risk	rs6022(A;A) rs6022(C;C) rs6022(T;T)
Alt	rs6022(A;A) rs6022(C;C) rs6022(T;T)
Reference	Rs6022(G;G)
Significance	Probable-non-pathogenic
Disease	not specified Thrombophilia Factor V deficiency Budd-Chiari syndrome Thrombophilia due to activated protein C resistance
Variation	info
Gene	F5
CLNDBN	not specified Thrombophilia Factor V deficiency Budd-Chiari syndrome Thrombophilia due to activated protein C resistance
Reversed	1
HGVS	NC_000001.10:g.169529826C>A
CLNSRC
CLNACC	RCV000249494.1, RCV000290429.1, RCV000305953.1, RCV000345339.1, RCV000394574.1,