rs878855032

Orientation

plus

Stabilized

plus

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

Make rs878855032(C;G)

Make rs878855032(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

8

Position

60830567

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs878855032
dbSNP (classic)	rs878855032
ClinGen	rs878855032
ebi	rs878855032
HLI	rs878855032
Exac	rs878855032
Gnomad	rs878855032
Varsome	rs878855032
LitVar	rs878855032
Map	rs878855032
PheGenI	rs878855032
Biobank	rs878855032
1000 genomes	rs878855032
hgdp	rs878855032
ensembl	rs878855032
geneview	rs878855032
scholar	rs878855032
google	rs878855032
pharmgkb	rs878855032
gwascentral	rs878855032
openSNP	rs878855032
23andMe	rs878855032
SNPshot	rs878855032
SNPdbe	rs878855032
MSV3d	rs878855032
GWAS Ctlg	rs878855032

Max Magnitude

0

ClinVar
Risk	rs878855032(G;G)
Alt	rs878855032(G;G)
Reference	Rs878855032(C;C)
Significance	Pathogenic
Disease	CHARGE association
Variation	info
Gene	CHD7
CLNDBN	CHARGE association
Reversed	0
HGVS	NC_000008.10:g.61743126C>G
CLNSRC
CLNACC	RCV000234220.1,