rs1060503182

Orientation

plus

Stabilized

plus

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

Make rs1060503182(C;C)

Make rs1060503182(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

60794985

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs1060503182
dbSNP (classic)	rs1060503182
ClinGen	rs1060503182
ebi	rs1060503182
HLI	rs1060503182
Exac	rs1060503182
Gnomad	rs1060503182
Varsome	rs1060503182
LitVar	rs1060503182
Map	rs1060503182
PheGenI	rs1060503182
Biobank	rs1060503182
1000 genomes	rs1060503182
hgdp	rs1060503182
ensembl	rs1060503182
geneview	rs1060503182
scholar	rs1060503182
google	rs1060503182
pharmgkb	rs1060503182
gwascentral	rs1060503182
openSNP	rs1060503182
23andMe	rs1060503182
SNPshot	rs1060503182
SNPdbe	rs1060503182
MSV3d	rs1060503182
GWAS Ctlg	rs1060503182

Max Magnitude

0

ClinVar
Risk	rs1060503182(C;C)
Alt	rs1060503182(C;C)
Reference	Rs1060503182(G;G)
Significance	Pathogenic
Disease	CHARGE association
Variation	info
Gene	CHD7
CLNDBN	CHARGE association
Reversed	0
HGVS	NC_000008.10:g.61707544G>C
CLNSRC
CLNACC	RCV000468880.1,