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rs587777759

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587777759(-;-)
Make rs587777759(-;T)
Make rs587777759(T;T)
ReferenceGRCh38 38.1/142
Chromosome22
Position20779633
GenePI4KA, SERPIND1
is asnp
is mentioned by
dbSNPrs587777759
ebirs587777759
HLIrs587777759
Exacrs587777759
Varsomers587777759
Maprs587777759
PheGenIrs587777759
hapmaprs587777759
1000 genomesrs587777759
hgdprs587777759
ensemblrs587777759
gopubmedrs587777759
geneviewrs587777759
scholarrs587777759
googlers587777759
pharmgkbrs587777759
gwascentralrs587777759
openSNPrs587777759
23andMers587777759
23andMe allrs587777759
SNP Nexus

SNPshotrs587777759
SNPdbers587777759
MSV3drs587777759
GWAS Ctlgrs587777759
Max Magnitude0
ClinVar
Risk rs587777759(T;T)
Alt rs587777759(T;T)
Reference rs587777759(;)
Significance Pathogenic
Disease Heparin cofactor II deficiency
Variation info
Gene SERPIND1 PI4KA
CLNDBN Heparin cofactor II deficiency
Reversed 0
HGVS NC_000022.10:g.21133921dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000016093.26,