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rs3024772

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs3024772(A;A)
Make rs3024772(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position113171786
GenePROZ
is asnp
is mentioned by
dbSNPrs3024772
ebirs3024772
HLIrs3024772
Exacrs3024772
Varsomers3024772
Maprs3024772
PheGenIrs3024772
hapmaprs3024772
1000 genomesrs3024772
hgdprs3024772
ensemblrs3024772
gopubmedrs3024772
geneviewrs3024772
scholarrs3024772
googlers3024772
pharmgkbrs3024772
gwascentralrs3024772
openSNPrs3024772
23andMers3024772
23andMe allrs3024772
SNP Nexus

SNPshotrs3024772
SNPdbers3024772
MSV3drs3024772
GWAS Ctlgrs3024772
GMAF0.02066
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 19050305] Association of the protein Z ATG haplotype with symptomatic nonvascular stroke or thromboembolism in white children: a family-based cohort study


GET Evidence
PROZ-R295H
aa_change Arg295His
aa_change_short R295H
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0254694
summary



[PMID 23420821] Protein Z variants associated with protein Z plasma levels and with risk of idiopathic recurrent miscarriage.