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rs387906894

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906894(A;G)
Make rs387906894(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position47683803
GeneCORIN
is asnp
is mentioned by
dbSNPrs387906894
ebirs387906894
HLIrs387906894
Exacrs387906894
Varsomers387906894
Maprs387906894
PheGenIrs387906894
hapmaprs387906894
1000 genomesrs387906894
hgdprs387906894
ensemblrs387906894
gopubmedrs387906894
geneviewrs387906894
scholarrs387906894
googlers387906894
pharmgkbrs387906894
gwascentralrs387906894
openSNPrs387906894
23andMers387906894
23andMe allrs387906894
SNP Nexus

SNPshotrs387906894
SNPdbers387906894
MSV3drs387906894
GWAS Ctlgrs387906894
Max Magnitude0
ClinVar
Risk rs387906894(G;G)
Alt rs387906894(G;G)
Reference rs387906894(A;A)
Significance Pathogenic
Disease Preeclampsia/eclampsia 5
Variation info
Gene CORIN
CLNDBN Preeclampsia/eclampsia 5
Reversed 1
HGVS NC_000004.11:g.47685820T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000023403.2,