rs863224843

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(I;I)	0	common genotype

Make rs863224843(-;-)

Make rs863224843(-;A)

Reference

GRCh38.p2 38.2/146

Chromosome

8

Position

60860958

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs863224843
dbSNP (classic)	rs863224843
ClinGen	rs863224843
ebi	rs863224843
HLI	rs863224843
Exac	rs863224843
Gnomad	rs863224843
Varsome	rs863224843
LitVar	rs863224843
Map	rs863224843
PheGenI	rs863224843
Biobank	rs863224843
1000 genomes	rs863224843
hgdp	rs863224843
ensembl	rs863224843
geneview	rs863224843
scholar	rs863224843
google	rs863224843
pharmgkb	rs863224843
gwascentral	rs863224843
openSNP	rs863224843
23andMe	rs863224843
SNPshot	rs863224843
SNPdbe	rs863224843
MSV3d	rs863224843
GWAS Ctlg	rs863224843

Max Magnitude

0

ClinVar
Risk	rs863224843(-;-)
Alt	rs863224843(-;-)
Reference	Rs863224843(A;A)
Significance	Pathogenic
Disease	CHARGE association
Variation	info
Gene	CHD7
CLNDBN	CHARGE association
Reversed	0
HGVS	NC_000008.10:g.61773517delA
CLNSRC
CLNACC	RCV000199327.1,