rs864622523

Orientation

plus

Stabilized

plus

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

Make rs864622523(A;C)

Make rs864622523(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

8

Position

60828661

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs864622523
dbSNP (classic)	rs864622523
ClinGen	rs864622523
ebi	rs864622523
HLI	rs864622523
Exac	rs864622523
Gnomad	rs864622523
Varsome	rs864622523
LitVar	rs864622523
Map	rs864622523
PheGenI	rs864622523
Biobank	rs864622523
1000 genomes	rs864622523
hgdp	rs864622523
ensembl	rs864622523
geneview	rs864622523
scholar	rs864622523
google	rs864622523
pharmgkb	rs864622523
gwascentral	rs864622523
openSNP	rs864622523
23andMe	rs864622523
SNPshot	rs864622523
SNPdbe	rs864622523
MSV3d	rs864622523
GWAS Ctlg	rs864622523

Max Magnitude

0

ClinVar
Risk	rs864622523(C;C)
Alt	rs864622523(C;C)
Reference	Rs864622523(A;A)
Significance	Probable-Pathogenic
Disease	CHARGE association
Variation	info
Gene	CHD7
CLNDBN	CHARGE association
Reversed	0
HGVS	NC_000008.10:g.61741220A>C
CLNSRC
CLNACC	RCV000205203.1,