rs1060503187

Orientation

plus

Stabilized

plus

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

Make rs1060503187(C;C)

Make rs1060503187(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

60822638

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs1060503187
dbSNP (classic)	rs1060503187
ClinGen	rs1060503187
ebi	rs1060503187
HLI	rs1060503187
Exac	rs1060503187
Gnomad	rs1060503187
Varsome	rs1060503187
LitVar	rs1060503187
Map	rs1060503187
PheGenI	rs1060503187
Biobank	rs1060503187
1000 genomes	rs1060503187
hgdp	rs1060503187
ensembl	rs1060503187
geneview	rs1060503187
scholar	rs1060503187
google	rs1060503187
pharmgkb	rs1060503187
gwascentral	rs1060503187
openSNP	rs1060503187
23andMe	rs1060503187
SNPshot	rs1060503187
SNPdbe	rs1060503187
MSV3d	rs1060503187
GWAS Ctlg	rs1060503187

Max Magnitude

0

ClinVar
Risk	rs1060503187(C;C)
Alt	rs1060503187(C;C)
Reference	Rs1060503187(G;G)
Significance	Pathogenic
Disease	CHARGE association
Variation	info
Gene	CHD7
CLNDBN	CHARGE association
Reversed	0
HGVS	NC_000008.10:g.61735197G>C
CLNSRC
CLNACC	RCV000464132.1,