rs1060499560

Orientation

plus

Stabilized

plus

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

Make rs1060499560(-;-)

Make rs1060499560(-;C)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

60853017

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs1060499560
dbSNP (classic)	rs1060499560
ClinGen	rs1060499560
ebi	rs1060499560
HLI	rs1060499560
Exac	rs1060499560
Gnomad	rs1060499560
Varsome	rs1060499560
LitVar	rs1060499560
Map	rs1060499560
PheGenI	rs1060499560
Biobank	rs1060499560
1000 genomes	rs1060499560
hgdp	rs1060499560
ensembl	rs1060499560
geneview	rs1060499560
scholar	rs1060499560
google	rs1060499560
pharmgkb	rs1060499560
gwascentral	rs1060499560
openSNP	rs1060499560
23andMe	rs1060499560
SNPshot	rs1060499560
SNPdbe	rs1060499560
MSV3d	rs1060499560
GWAS Ctlg	rs1060499560

Max Magnitude

0

ClinVar
Risk	rs1060499560(-;-)
Alt	rs1060499560(-;-)
Reference	Rs1060499560(C;C)
Significance	Pathogenic
Disease	CHARGE association
Variation	info
Gene	CHD7
CLNDBN	CHARGE association
Reversed	0
HGVS	NC_000008.10:g.61765576delC
CLNSRC
CLNACC	RCV000474707.1,