rs727503860

Orientation

plus

Stabilized

plus

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

Make rs727503860(C;T)

Make rs727503860(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

8

Position

60742522

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs727503860
dbSNP (classic)	rs727503860
ClinGen	rs727503860
ebi	rs727503860
HLI	rs727503860
Exac	rs727503860
Gnomad	rs727503860
Varsome	rs727503860
LitVar	rs727503860
Map	rs727503860
PheGenI	rs727503860
Biobank	rs727503860
1000 genomes	rs727503860
hgdp	rs727503860
ensembl	rs727503860
geneview	rs727503860
scholar	rs727503860
google	rs727503860
pharmgkb	rs727503860
gwascentral	rs727503860
openSNP	rs727503860
23andMe	rs727503860
SNPshot	rs727503860
SNPdbe	rs727503860
MSV3d	rs727503860
GWAS Ctlg	rs727503860

Max Magnitude

0

ClinVar
Risk	rs727503860(T;T)
Alt	rs727503860(T;T)
Reference	Rs727503860(C;C)
Significance	Pathogenic
Disease	not provided CHARGE association
Variation	info
Gene	CHD7
CLNDBN	not provided CHARGE association
Reversed	0
HGVS	NC_000008.10:g.61655081C>T
CLNSRC
CLNACC	RCV000153004.3, RCV000405637.1,