rs387906894

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs387906894(A;G)

Make rs387906894(G;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

47683803

Gene

CORIN

is a	snp
is	mentioned by
dbSNP	rs387906894
dbSNP (classic)	rs387906894
ClinGen	rs387906894
ebi	rs387906894
HLI	rs387906894
Exac	rs387906894
Gnomad	rs387906894
Varsome	rs387906894
LitVar	rs387906894
Map	rs387906894
PheGenI	rs387906894
Biobank	rs387906894
1000 genomes	rs387906894
hgdp	rs387906894
ensembl	rs387906894
geneview	rs387906894
scholar	rs387906894
google	rs387906894
pharmgkb	rs387906894
gwascentral	rs387906894
openSNP	rs387906894
23andMe	rs387906894
SNPshot	rs387906894
SNPdbe	rs387906894
MSV3d	rs387906894
GWAS Ctlg	rs387906894

Max Magnitude

0

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 UniProtKB (protein)
CLNACC	RCV000023403.2,