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rs6028

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs6028(C;C)
Make rs6028(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position169582444
GeneF5
is asnp
is mentioned by
dbSNPrs6028
dbSNP (classic)rs6028
ClinGenrs6028
ebirs6028
HLIrs6028
Exacrs6028
Gnomadrs6028
Varsomers6028
LitVarrs6028
Maprs6028
PheGenIrs6028
Biobankrs6028
1000 genomesrs6028
hgdprs6028
ensemblrs6028
geneviewrs6028
scholarrs6028
googlers6028
pharmgkbrs6028
gwascentralrs6028
openSNPrs6028
23andMers6028
SNPshotrs6028
SNPdbers6028
MSV3drs6028
GWAS Ctlgrs6028
GMAF0.2282
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 22703881OA-icon.png]
Trait
Title Genetic Associations for Activated Partial Thromboplastin Time and Prothrombin Time, their Gene Expression Profiles, and Risk of Coronary Artery Disease.
Risk Allele C
P-val 3E-9
Odds Ratio 0.2260 None


[PMID 18426996OA-icon.png] Relations of inflammatory biomarkers and common genetic variants with arterial stiffness and wave reflection.


[PMID 19404301OA-icon.png] Variation in the upstream region of P-Selectin (SELP) is a risk factor for SLE.


ClinVar
Risk rs6028(C;C)
Alt rs6028(C;C)
Reference Rs6028(T;T)
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 0
HGVS NC_000001.10:g.169551682T>C
CLNSRC
CLNACC RCV000243137.1, RCV000271943.1, RCV000311703.1, RCV000327005.1, RCV000366465.1,