rs587783455

Orientation

plus

Stabilized

plus

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

Make rs587783455(C;T)

Make rs587783455(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

8

Position

60856532

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs587783455
dbSNP (classic)	rs587783455
ClinGen	rs587783455
ebi	rs587783455
HLI	rs587783455
Exac	rs587783455
Gnomad	rs587783455
Varsome	rs587783455
LitVar	rs587783455
Map	rs587783455
PheGenI	rs587783455
Biobank	rs587783455
1000 genomes	rs587783455
hgdp	rs587783455
ensembl	rs587783455
geneview	rs587783455
scholar	rs587783455
google	rs587783455
pharmgkb	rs587783455
gwascentral	rs587783455
openSNP	rs587783455
23andMe	rs587783455
SNPshot	rs587783455
SNPdbe	rs587783455
MSV3d	rs587783455
GWAS Ctlg	rs587783455

Max Magnitude

0

ClinVar
Risk	rs587783455(T;T)
Alt	rs587783455(T;T)
Reference	Rs587783455(C;C)
Significance	Pathogenic
Disease	CHARGE association
Variation	info
Gene	CHD7
CLNDBN	CHARGE association
Reversed	0
HGVS	NC_000008.10:g.61769091C>T
CLNSRC
CLNACC	RCV000145690.1,