rs587783459

Orientation

plus

Stabilized

plus

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

Make rs587783459(A;A)

Make rs587783459(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

8

Position

60862631

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs587783459
dbSNP (classic)	rs587783459
ClinGen	rs587783459
ebi	rs587783459
HLI	rs587783459
Exac	rs587783459
Gnomad	rs587783459
Varsome	rs587783459
LitVar	rs587783459
Map	rs587783459
PheGenI	rs587783459
Biobank	rs587783459
1000 genomes	rs587783459
hgdp	rs587783459
ensembl	rs587783459
geneview	rs587783459
scholar	rs587783459
google	rs587783459
pharmgkb	rs587783459
gwascentral	rs587783459
openSNP	rs587783459
23andMe	rs587783459
SNPshot	rs587783459
SNPdbe	rs587783459
MSV3d	rs587783459
GWAS Ctlg	rs587783459

Max Magnitude

0

ClinVar
Risk	rs587783459(A;A)
Alt	rs587783459(A;A)
Reference	Rs587783459(G;G)
Significance	Pathogenic
Disease	CHARGE association
Variation	info
Gene	CHD7
CLNDBN	CHARGE association
Reversed	0
HGVS	NC_000008.10:g.61775190G>A
CLNSRC
CLNACC	RCV000145698.1,