rs878855031

Orientation

plus

Stabilized

plus

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

Make rs878855031(A;T)

Make rs878855031(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

8

Position

60822022

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs878855031
dbSNP (classic)	rs878855031
ClinGen	rs878855031
ebi	rs878855031
HLI	rs878855031
Exac	rs878855031
Gnomad	rs878855031
Varsome	rs878855031
LitVar	rs878855031
Map	rs878855031
PheGenI	rs878855031
Biobank	rs878855031
1000 genomes	rs878855031
hgdp	rs878855031
ensembl	rs878855031
geneview	rs878855031
scholar	rs878855031
google	rs878855031
pharmgkb	rs878855031
gwascentral	rs878855031
openSNP	rs878855031
23andMe	rs878855031
SNPshot	rs878855031
SNPdbe	rs878855031
MSV3d	rs878855031
GWAS Ctlg	rs878855031

Max Magnitude

0

ClinVar
Risk	rs878855031(T;T)
Alt	rs878855031(T;T)
Reference	Rs878855031(A;A)
Significance	Probable-Pathogenic
Disease	CHARGE association
Variation	info
Gene	CHD7
CLNDBN	CHARGE association
Reversed	0
HGVS	NC_000008.10:g.61734581A>T
CLNSRC
CLNACC	RCV000232661.1,