rs587783436

Orientation

plus

Stabilized

plus

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

Make rs587783436(-;-)

Make rs587783436(-;AG)

Reference

GRCh38.p2 38.2/144

Chromosome

8

Position

60822093

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs587783436
dbSNP (classic)	rs587783436
ClinGen	rs587783436
ebi	rs587783436
HLI	rs587783436
Exac	rs587783436
Gnomad	rs587783436
Varsome	rs587783436
LitVar	rs587783436
Map	rs587783436
PheGenI	rs587783436
Biobank	rs587783436
1000 genomes	rs587783436
hgdp	rs587783436
ensembl	rs587783436
geneview	rs587783436
scholar	rs587783436
google	rs587783436
pharmgkb	rs587783436
gwascentral	rs587783436
openSNP	rs587783436
23andMe	rs587783436
SNPshot	rs587783436
SNPdbe	rs587783436
MSV3d	rs587783436
GWAS Ctlg	rs587783436

Max Magnitude

0

ClinVar
Risk	rs587783436(-;-)
Alt	rs587783436(-;-)
Reference	Rs587783436(AG;AG)
Significance	Pathogenic
Disease	CHARGE association not provided
Variation	info
Gene	CHD7
CLNDBN	CHARGE association not provided
Reversed	0
HGVS	NC_000008.10:g.61734652_61734653delAG
CLNSRC
CLNACC	RCV000145662.1, RCV000443611.1,