rs587783447

Orientation

plus

Stabilized

plus

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

Make rs587783447(G;T)

Make rs587783447(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

8

Position

60851048

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs587783447
dbSNP (classic)	rs587783447
ClinGen	rs587783447
ebi	rs587783447
HLI	rs587783447
Exac	rs587783447
Gnomad	rs587783447
Varsome	rs587783447
LitVar	rs587783447
Map	rs587783447
PheGenI	rs587783447
Biobank	rs587783447
1000 genomes	rs587783447
hgdp	rs587783447
ensembl	rs587783447
geneview	rs587783447
scholar	rs587783447
google	rs587783447
pharmgkb	rs587783447
gwascentral	rs587783447
openSNP	rs587783447
23andMe	rs587783447
SNPshot	rs587783447
SNPdbe	rs587783447
MSV3d	rs587783447
GWAS Ctlg	rs587783447

Max Magnitude

0

ClinVar
Risk	rs587783447(T;T)
Alt	rs587783447(T;T)
Reference	Rs587783447(G;G)
Significance	Pathogenic
Disease	CHARGE association
Variation	info
Gene	CHD7
CLNDBN	CHARGE association
Reversed	0
HGVS	NC_000008.10:g.61763607G>T
CLNSRC
CLNACC	RCV000145678.1,