Have questions? Visit https://www.reddit.com/r/SNPedia

rs9898

From SNPedia

Orientationplus
Stabilizedplus
Make rs9898(C;C)
Make rs9898(C;T)
Make rs9898(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position186672838
GeneHRG
is asnp
is mentioned by
dbSNPrs9898
ebirs9898
HLIrs9898
Exacrs9898
Varsomers9898
Maprs9898
PheGenIrs9898
hapmaprs9898
1000 genomesrs9898
hgdprs9898
ensemblrs9898
gopubmedrs9898
geneviewrs9898
scholarrs9898
googlers9898
pharmgkbrs9898
gwascentralrs9898
openSNPrs9898
23andMers9898
23andMe allrs9898
SNP Nexus

SNPshotrs9898
SNPdbers9898
MSV3drs9898
GWAS Ctlgrs9898
GMAF0.4633
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20303064OA-icon.png]
Trait Activated partial thromboplastin time
Title Common Variants of Large Effect in F12, KNG1, and HRG Are Associated with Activated Partial Thromboplastin Time
Risk Allele T
P-val 1E-11
Odds Ratio 0.26 [0.19-0.33] unit increase
OMIM142640
DescHISTIDINE-RICH GLYCOPROTEIN; HRG
Variant
Relatedalso
OMIM188050
Desc
Variant
Relatedalso

[PMID 21270443] KNG1 Ile581Thr and susceptibility to venous thrombosis.

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 1E-111
Odds Ratio 1.0000 None


GET Evidence
HRG-P204S
aa_change Pro204Ser
aa_change_short P204S
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.429169
summary