rs28942092

Orientation

plus

Stabilized

plus

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

Make rs28942092(C;T)

Make rs28942092(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

9943399

Gene

CRELD1

is a	snp
is	mentioned by
dbSNP	rs28942092
dbSNP (classic)	rs28942092
ClinGen	rs28942092
ebi	rs28942092
HLI	rs28942092
Exac	rs28942092
Gnomad	rs28942092
Varsome	rs28942092
LitVar	rs28942092
Map	rs28942092
PheGenI	rs28942092
Biobank	rs28942092
1000 genomes	rs28942092
hgdp	rs28942092
ensembl	rs28942092
geneview	rs28942092
scholar	rs28942092
google	rs28942092
pharmgkb	rs28942092
gwascentral	rs28942092
openSNP	rs28942092
23andMe	rs28942092
SNPshot	rs28942092
SNPdbe	rs28942092
MSV3d	rs28942092
GWAS Ctlg	rs28942092

GMAF

0.0004591

Max Magnitude

0

OMIM	607170
Desc	ATRIOVENTRICULAR SEPTAL DEFECT, SUSCEPTIBILITY TO, 2
Variant	0002
Related	also

ClinVar
Risk	rs28942092(T;T)
Alt	rs28942092(T;T)
Reference	Rs28942092(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.9985083C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000003597.2,