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rs387906895

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906895(A;G)
Make rs387906895(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position47665207
GeneCORIN
is asnp
is mentioned by
dbSNPrs387906895
ebirs387906895
HLIrs387906895
Exacrs387906895
Varsomers387906895
Maprs387906895
PheGenIrs387906895
hapmaprs387906895
1000 genomesrs387906895
hgdprs387906895
ensemblrs387906895
gopubmedrs387906895
geneviewrs387906895
scholarrs387906895
googlers387906895
pharmgkbrs387906895
gwascentralrs387906895
openSNPrs387906895
23andMers387906895
23andMe allrs387906895
SNP Nexus

SNPshotrs387906895
SNPdbers387906895
MSV3drs387906895
GWAS Ctlgrs387906895
Max Magnitude0
ClinVar
Risk rs387906895(G;G)
Alt rs387906895(G;G)
Reference rs387906895(A;A)
Significance Pathogenic
Disease Preeclampsia/eclampsia 5
Variation info
Gene CORIN
CLNDBN Preeclampsia/eclampsia 5
Reversed 1
HGVS NC_000004.11:g.47667224T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000023404.2,