rs1060503184

Orientation

plus

Stabilized

plus

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

Make rs1060503184(-;-)

Make rs1060503184(-;T)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

60742490

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs1060503184
dbSNP (classic)	rs1060503184
ClinGen	rs1060503184
ebi	rs1060503184
HLI	rs1060503184
Exac	rs1060503184
Gnomad	rs1060503184
Varsome	rs1060503184
LitVar	rs1060503184
Map	rs1060503184
PheGenI	rs1060503184
Biobank	rs1060503184
1000 genomes	rs1060503184
hgdp	rs1060503184
ensembl	rs1060503184
geneview	rs1060503184
scholar	rs1060503184
google	rs1060503184
pharmgkb	rs1060503184
gwascentral	rs1060503184
openSNP	rs1060503184
23andMe	rs1060503184
SNPshot	rs1060503184
SNPdbe	rs1060503184
MSV3d	rs1060503184
GWAS Ctlg	rs1060503184

Max Magnitude

0

ClinVar
Risk	rs1060503184(-;-)
Alt	rs1060503184(-;-)
Reference	Rs1060503184(T;T)
Significance	Pathogenic
Disease	CHARGE association
Variation	info
Gene	CHD7
CLNDBN	CHARGE association
Reversed	0
HGVS	NC_000008.10:g.61655049delT
CLNSRC
CLNACC	RCV000467254.1,