rs863224856

Orientation

plus

Stabilized

plus

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

Make rs863224856(-;T)

Make rs863224856(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

8

Position

60845398

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs863224856
dbSNP (classic)	rs863224856
ClinGen	rs863224856
ebi	rs863224856
HLI	rs863224856
Exac	rs863224856
Gnomad	rs863224856
Varsome	rs863224856
LitVar	rs863224856
Map	rs863224856
PheGenI	rs863224856
Biobank	rs863224856
1000 genomes	rs863224856
hgdp	rs863224856
ensembl	rs863224856
geneview	rs863224856
scholar	rs863224856
google	rs863224856
pharmgkb	rs863224856
gwascentral	rs863224856
openSNP	rs863224856
23andMe	rs863224856
SNPshot	rs863224856
SNPdbe	rs863224856
MSV3d	rs863224856
GWAS Ctlg	rs863224856

Max Magnitude

0

ClinVar
Risk	rs863224856(T;T)
Alt	rs863224856(T;T)
Reference	Rs863224856(-;-)
Significance	Pathogenic
Disease	CHARGE association
Variation	info
Gene	CHD7
CLNDBN	CHARGE association
Reversed	0
HGVS	NC_000008.10:g.61757957dupT
CLNSRC
CLNACC	RCV000198147.1,