rs1060503183

Orientation

plus

Stabilized

plus

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

Make rs1060503183(G;G)

Make rs1060503183(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

60823837

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs1060503183
dbSNP (classic)	rs1060503183
ClinGen	rs1060503183
ebi	rs1060503183
HLI	rs1060503183
Exac	rs1060503183
Gnomad	rs1060503183
Varsome	rs1060503183
LitVar	rs1060503183
Map	rs1060503183
PheGenI	rs1060503183
Biobank	rs1060503183
1000 genomes	rs1060503183
hgdp	rs1060503183
ensembl	rs1060503183
geneview	rs1060503183
scholar	rs1060503183
google	rs1060503183
pharmgkb	rs1060503183
gwascentral	rs1060503183
openSNP	rs1060503183
23andMe	rs1060503183
SNPshot	rs1060503183
SNPdbe	rs1060503183
MSV3d	rs1060503183
GWAS Ctlg	rs1060503183

Max Magnitude

0

ClinVar
Risk	rs1060503183(G;G)
Alt	rs1060503183(G;G)
Reference	Rs1060503183(T;T)
Significance	Pathogenic
Disease	CHARGE association
Variation	info
Gene	CHD7
CLNDBN	CHARGE association
Reversed	0
HGVS	NC_000008.10:g.61736396T>G
CLNSRC
CLNACC	RCV000460607.1,