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rs6022

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs6022(G;T)
Make rs6022(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position169560588
GeneF5
is asnp
is mentioned by
dbSNPrs6022
ClinGenrs6022
ebirs6022
HLIrs6022
Exacrs6022
Varsomers6022
Maprs6022
PheGenIrs6022
hapmaprs6022
1000 genomesrs6022
hgdprs6022
ensemblrs6022
gopubmedrs6022
geneviewrs6022
scholarrs6022
googlers6022
pharmgkbrs6022
gwascentralrs6022
openSNPrs6022
23andMers6022
23andMe allrs6022
SNP Nexus

SNPshotrs6022
SNPdbers6022
MSV3drs6022
GWAS Ctlgrs6022
GMAF0.4132
Max Magnitude0
? (G;G) (G;T) (T;T) 28
[PMID 19020903OA-icon.png] 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,