rs587783442

Orientation

plus

Stabilized

plus

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

Make rs587783442(C;T)

Make rs587783442(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

8

Position

60838202

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs587783442
dbSNP (classic)	rs587783442
ClinGen	rs587783442
ebi	rs587783442
HLI	rs587783442
Exac	rs587783442
Gnomad	rs587783442
Varsome	rs587783442
LitVar	rs587783442
Map	rs587783442
PheGenI	rs587783442
Biobank	rs587783442
1000 genomes	rs587783442
hgdp	rs587783442
ensembl	rs587783442
geneview	rs587783442
scholar	rs587783442
google	rs587783442
pharmgkb	rs587783442
gwascentral	rs587783442
openSNP	rs587783442
23andMe	rs587783442
SNPshot	rs587783442
SNPdbe	rs587783442
MSV3d	rs587783442
GWAS Ctlg	rs587783442

Max Magnitude

0

ClinVar
Risk	rs587783442(T;T)
Alt	rs587783442(T;T)
Reference	Rs587783442(C;C)
Significance	Pathogenic
Disease	CHARGE association
Variation	info
Gene	CHD7
CLNDBN	CHARGE association
Reversed	0
HGVS	NC_000008.10:g.61750761C>T
CLNSRC
CLNACC	RCV000145671.2,