rs1060503185

Orientation

plus

Stabilized

plus

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

Make rs1060503185(-;-)

Make rs1060503185(-;CT)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

60852888

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs1060503185
dbSNP (classic)	rs1060503185
ClinGen	rs1060503185
ebi	rs1060503185
HLI	rs1060503185
Exac	rs1060503185
Gnomad	rs1060503185
Varsome	rs1060503185
LitVar	rs1060503185
Map	rs1060503185
PheGenI	rs1060503185
Biobank	rs1060503185
1000 genomes	rs1060503185
hgdp	rs1060503185
ensembl	rs1060503185
geneview	rs1060503185
scholar	rs1060503185
google	rs1060503185
pharmgkb	rs1060503185
gwascentral	rs1060503185
openSNP	rs1060503185
23andMe	rs1060503185
SNPshot	rs1060503185
SNPdbe	rs1060503185
MSV3d	rs1060503185
GWAS Ctlg	rs1060503185

Max Magnitude

0

ClinVar
Risk	rs1060503185(-;-)
Alt	rs1060503185(-;-)
Reference	Rs1060503185(CT;CT)
Significance	Pathogenic
Disease	CHARGE association
Variation	info
Gene	CHD7
CLNDBN	CHARGE association
Reversed	0
HGVS	NC_000008.10:g.61765447_61765448delCT
CLNSRC
CLNACC	RCV000475738.1,