rs879255410

Orientation

plus

Stabilized

plus

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

Make rs879255410(-;-)

Make rs879255410(-;C)

Reference

GRCh38.p2 38.2/147

Chromosome

8

Position

60836258

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs879255410
dbSNP (classic)	rs879255410
ClinGen	rs879255410
ebi	rs879255410
HLI	rs879255410
Exac	rs879255410
Gnomad	rs879255410
Varsome	rs879255410
LitVar	rs879255410
Map	rs879255410
PheGenI	rs879255410
Biobank	rs879255410
1000 genomes	rs879255410
hgdp	rs879255410
ensembl	rs879255410
geneview	rs879255410
scholar	rs879255410
google	rs879255410
pharmgkb	rs879255410
gwascentral	rs879255410
openSNP	rs879255410
23andMe	rs879255410
SNPshot	rs879255410
SNPdbe	rs879255410
MSV3d	rs879255410
GWAS Ctlg	rs879255410

Max Magnitude

0

ClinVar
Risk	rs879255410(-;-)
Alt	rs879255410(-;-)
Reference	Rs879255410(C;C)
Significance	Pathogenic
Disease	not provided CHARGE association
Variation	info
Gene	CHD7
CLNDBN	not provided CHARGE association
Reversed	0
HGVS	NC_000008.10:g.61748817delC
CLNSRC
CLNACC	RCV000238786.1, RCV000258139.1,