rs28942091

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs28942091(C;T)

Make rs28942091(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

9943452

Gene

CRELD1

is a	snp
is	mentioned by
dbSNP	rs28942091
dbSNP (classic)	rs28942091
ClinGen	rs28942091
ebi	rs28942091
HLI	rs28942091
Exac	rs28942091
Gnomad	rs28942091
Varsome	rs28942091
LitVar	rs28942091
Map	rs28942091
PheGenI	rs28942091
Biobank	rs28942091
1000 genomes	rs28942091
hgdp	rs28942091
ensembl	rs28942091
geneview	rs28942091
scholar	rs28942091
google	rs28942091
pharmgkb	rs28942091
gwascentral	rs28942091
openSNP	rs28942091
23andMe	rs28942091
SNPshot	rs28942091
SNPdbe	rs28942091
MSV3d	rs28942091
GWAS Ctlg	rs28942091

GMAF

0.0004591

Max Magnitude

0

OMIM	607170
Desc	ATRIOVENTRICULAR SEPTAL DEFECT, SUSCEPTIBILITY TO, 2
Variant	0001
Related	also

ClinVar
Risk	rs28942091(G;G) rs28942091(T;T)
Alt	rs28942091(G;G) rs28942091(T;T)
Reference	Rs28942091(C;C)
Significance	Other
Disease	Atrioventricular septal defect 2
Variation	info
Gene	CRELD1
CLNDBN	Atrioventricular septal defect 2
Reversed	0
HGVS	NC_000003.11:g.9985136C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000003596.3,