rs1060503181

Orientation

plus

Stabilized

plus

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

Make rs1060503181(-;-)

Make rs1060503181(-;T)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

60816456

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs1060503181
dbSNP (classic)	rs1060503181
ClinGen	rs1060503181
ebi	rs1060503181
HLI	rs1060503181
Exac	rs1060503181
Gnomad	rs1060503181
Varsome	rs1060503181
LitVar	rs1060503181
Map	rs1060503181
PheGenI	rs1060503181
Biobank	rs1060503181
1000 genomes	rs1060503181
hgdp	rs1060503181
ensembl	rs1060503181
geneview	rs1060503181
scholar	rs1060503181
google	rs1060503181
pharmgkb	rs1060503181
gwascentral	rs1060503181
openSNP	rs1060503181
23andMe	rs1060503181
SNPshot	rs1060503181
SNPdbe	rs1060503181
MSV3d	rs1060503181
GWAS Ctlg	rs1060503181

Max Magnitude

0

ClinVar
Risk	rs1060503181(-;-)
Alt	rs1060503181(-;-)
Reference	Rs1060503181(T;T)
Significance	Pathogenic
Disease	CHARGE association
Variation	info
Gene	CHD7
CLNDBN	CHARGE association
Reversed	0
HGVS	NC_000008.10:g.61729015delT
CLNSRC
CLNACC	RCV000464453.1,