rs587783448

Orientation

plus

Stabilized

plus

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

Make rs587783448(A;C)

Make rs587783448(C;C)

Reference

GRCh38.p2 38.2/144

Chromosome

8

Position

60852017

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs587783448
dbSNP (classic)	rs587783448
ClinGen	rs587783448
ebi	rs587783448
HLI	rs587783448
Exac	rs587783448
Gnomad	rs587783448
Varsome	rs587783448
LitVar	rs587783448
Map	rs587783448
PheGenI	rs587783448
Biobank	rs587783448
1000 genomes	rs587783448
hgdp	rs587783448
ensembl	rs587783448
geneview	rs587783448
scholar	rs587783448
google	rs587783448
pharmgkb	rs587783448
gwascentral	rs587783448
openSNP	rs587783448
23andMe	rs587783448
SNPshot	rs587783448
SNPdbe	rs587783448
MSV3d	rs587783448
GWAS Ctlg	rs587783448

Max Magnitude

0

ClinVar
Risk	rs587783448(C;C)
Alt	rs587783448(C;C)
Reference	Rs587783448(A;A)
Significance	Pathogenic
Disease	CHARGE association
Variation	info
Gene	CHD7
CLNDBN	CHARGE association
Reversed	0
HGVS	NC_000008.10:g.61764576A>C
CLNSRC
CLNACC	RCV000145679.1,