rs1060503180

Orientation

plus

Stabilized

plus

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

Make rs1060503180(C;C)

Make rs1060503180(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

60848514

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs1060503180
dbSNP (classic)	rs1060503180
ClinGen	rs1060503180
ebi	rs1060503180
HLI	rs1060503180
Exac	rs1060503180
Gnomad	rs1060503180
Varsome	rs1060503180
LitVar	rs1060503180
Map	rs1060503180
PheGenI	rs1060503180
Biobank	rs1060503180
1000 genomes	rs1060503180
hgdp	rs1060503180
ensembl	rs1060503180
geneview	rs1060503180
scholar	rs1060503180
google	rs1060503180
pharmgkb	rs1060503180
gwascentral	rs1060503180
openSNP	rs1060503180
23andMe	rs1060503180
SNPshot	rs1060503180
SNPdbe	rs1060503180
MSV3d	rs1060503180
GWAS Ctlg	rs1060503180

Max Magnitude

0

ClinVar
Risk	rs1060503180(C;C)
Alt	rs1060503180(C;C)
Reference	Rs1060503180(G;G)
Significance	Pathogenic
Disease	CHARGE association
Variation	info
Gene	CHD7
CLNDBN	CHARGE association
Reversed	0
HGVS	NC_000008.10:g.61761073G>C
CLNSRC
CLNACC	RCV000457833.1,