rs1060503188

Orientation

plus

Stabilized

plus

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

Make rs1060503188(C;T)

Make rs1060503188(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

60856592

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs1060503188
dbSNP (classic)	rs1060503188
ClinGen	rs1060503188
ebi	rs1060503188
HLI	rs1060503188
Exac	rs1060503188
Gnomad	rs1060503188
Varsome	rs1060503188
LitVar	rs1060503188
Map	rs1060503188
PheGenI	rs1060503188
Biobank	rs1060503188
1000 genomes	rs1060503188
hgdp	rs1060503188
ensembl	rs1060503188
geneview	rs1060503188
scholar	rs1060503188
google	rs1060503188
pharmgkb	rs1060503188
gwascentral	rs1060503188
openSNP	rs1060503188
23andMe	rs1060503188
SNPshot	rs1060503188
SNPdbe	rs1060503188
MSV3d	rs1060503188
GWAS Ctlg	rs1060503188

Max Magnitude

0

ClinVar
Risk	rs1060503188(T;T)
Alt	rs1060503188(T;T)
Reference	Rs1060503188(C;C)
Significance	Pathogenic
Disease	CHARGE association
Variation	info
Gene	CHD7
CLNDBN	CHARGE association
Reversed	0
HGVS	NC_000008.10:g.61769151C>T
CLNSRC
CLNACC	RCV000469838.1,