rs797045469

Orientation

plus

Stabilized

plus

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

Make rs797045469(-;G)

Make rs797045469(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

8

Position

60851292

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs797045469
dbSNP (classic)	rs797045469
ClinGen	rs797045469
ebi	rs797045469
HLI	rs797045469
Exac	rs797045469
Gnomad	rs797045469
Varsome	rs797045469
LitVar	rs797045469
Map	rs797045469
PheGenI	rs797045469
Biobank	rs797045469
1000 genomes	rs797045469
hgdp	rs797045469
ensembl	rs797045469
geneview	rs797045469
scholar	rs797045469
google	rs797045469
pharmgkb	rs797045469
gwascentral	rs797045469
openSNP	rs797045469
23andMe	rs797045469
SNPshot	rs797045469
SNPdbe	rs797045469
MSV3d	rs797045469
GWAS Ctlg	rs797045469

Max Magnitude

0

ClinVar
Risk	rs797045469(G;G)
Alt	rs797045469(G;G)
Reference	Rs797045469(-;-)
Significance	Pathogenic
Disease	CHARGE association
Variation	info
Gene	CHD7
CLNDBN	CHARGE association
Reversed	0
HGVS	NC_000008.10:g.61763851dupG
CLNSRC
CLNACC	RCV000195102.1,