rs267606724

Orientation

plus

Stabilized

plus

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

Make rs267606724(C;T)

Make rs267606724(T;T)

Reference

GRCh38 38.1/141

Chromosome

8

Position

60841997

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs267606724
dbSNP (classic)	rs267606724
ClinGen	rs267606724
ebi	rs267606724
HLI	rs267606724
Exac	rs267606724
Gnomad	rs267606724
Varsome	rs267606724
LitVar	rs267606724
Map	rs267606724
PheGenI	rs267606724
Biobank	rs267606724
1000 genomes	rs267606724
hgdp	rs267606724
ensembl	rs267606724
geneview	rs267606724
scholar	rs267606724
google	rs267606724
pharmgkb	rs267606724
gwascentral	rs267606724
openSNP	rs267606724
23andMe	rs267606724
SNPshot	rs267606724
SNPdbe	rs267606724
MSV3d	rs267606724
GWAS Ctlg	rs267606724

Max Magnitude

0

ClinVar
Risk	rs267606724(G;G) rs267606724(T;T)
Alt	rs267606724(G;G) rs267606724(T;T)
Reference	Rs267606724(C;C)
Significance	Pathogenic
Disease	CHARGE association not provided
Variation	info
Gene	CHD7
CLNDBN	CHARGE association not provided
Reversed	0
HGVS	NC_000008.10:g.61754556C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000002118.2, RCV000122607.2,