rs797045461

Orientation

plus

Stabilized

plus

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

Make rs797045461(-;G)

Make rs797045461(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

8

Position

60781012

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs797045461
dbSNP (classic)	rs797045461
ClinGen	rs797045461
ebi	rs797045461
HLI	rs797045461
Exac	rs797045461
Gnomad	rs797045461
Varsome	rs797045461
LitVar	rs797045461
Map	rs797045461
PheGenI	rs797045461
Biobank	rs797045461
1000 genomes	rs797045461
hgdp	rs797045461
ensembl	rs797045461
geneview	rs797045461
scholar	rs797045461
google	rs797045461
pharmgkb	rs797045461
gwascentral	rs797045461
openSNP	rs797045461
23andMe	rs797045461
SNPshot	rs797045461
SNPdbe	rs797045461
MSV3d	rs797045461
GWAS Ctlg	rs797045461

Max Magnitude

0

ClinVar
Risk	rs797045461(G;G)
Alt	rs797045461(G;G)
Reference	Rs797045461(-;-)
Significance	Pathogenic
Disease	CHARGE association
Variation	info
Gene	CHD7
CLNDBN	CHARGE association
Reversed	0
HGVS	NC_000008.10:g.61693571dupG
CLNSRC
CLNACC	RCV000194479.1,