rs1060503189

Orientation

plus

Stabilized

plus

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

Make rs1060503189(-;-)

Make rs1060503189(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

60816502

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs1060503189
dbSNP (classic)	rs1060503189
ClinGen	rs1060503189
ebi	rs1060503189
HLI	rs1060503189
Exac	rs1060503189
Gnomad	rs1060503189
Varsome	rs1060503189
LitVar	rs1060503189
Map	rs1060503189
PheGenI	rs1060503189
Biobank	rs1060503189
1000 genomes	rs1060503189
hgdp	rs1060503189
ensembl	rs1060503189
geneview	rs1060503189
scholar	rs1060503189
google	rs1060503189
pharmgkb	rs1060503189
gwascentral	rs1060503189
openSNP	rs1060503189
23andMe	rs1060503189
SNPshot	rs1060503189
SNPdbe	rs1060503189
MSV3d	rs1060503189
GWAS Ctlg	rs1060503189

Max Magnitude

0

ClinVar
Risk	rs1060503189(-;-)
Alt	rs1060503189(-;-)
Reference	Rs1060503189(G;G)
Significance	Probable-Pathogenic
Disease	CHARGE association
Variation	info
Gene	CHD7
CLNDBN	CHARGE association
Reversed	0
HGVS	NC_000008.10:g.61729061delG
CLNSRC
CLNACC	RCV000457698.1,