rs398124320

Orientation

plus

Stabilized

plus

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

Make rs398124320(C;G)

Make rs398124320(G;G)

Reference

GRCh38 38.1/141

Chromosome

8

Position

60845380

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs398124320
dbSNP (classic)	rs398124320
ClinGen	rs398124320
ebi	rs398124320
HLI	rs398124320
Exac	rs398124320
Gnomad	rs398124320
Varsome	rs398124320
LitVar	rs398124320
Map	rs398124320
PheGenI	rs398124320
Biobank	rs398124320
1000 genomes	rs398124320
hgdp	rs398124320
ensembl	rs398124320
geneview	rs398124320
scholar	rs398124320
google	rs398124320
pharmgkb	rs398124320
gwascentral	rs398124320
openSNP	rs398124320
23andMe	rs398124320
SNPshot	rs398124320
SNPdbe	rs398124320
MSV3d	rs398124320
GWAS Ctlg	rs398124320

Max Magnitude

0

ClinVar
Risk	rs398124320(G;G) rs398124320(T;T)
Alt	rs398124320(G;G) rs398124320(T;T)
Reference	Rs398124320(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.61757939C>G
CLNSRC	ClinVar Emory University
CLNACC	RCV000081839.4, RCV000352992.1,