rs1057521078

Orientation

plus

Stabilized

plus

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

Make rs1057521078(A;G)

Make rs1057521078(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

60841989

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs1057521078
dbSNP (classic)	rs1057521078
ClinGen	rs1057521078
ebi	rs1057521078
HLI	rs1057521078
Exac	rs1057521078
Gnomad	rs1057521078
Varsome	rs1057521078
LitVar	rs1057521078
Map	rs1057521078
PheGenI	rs1057521078
Biobank	rs1057521078
1000 genomes	rs1057521078
hgdp	rs1057521078
ensembl	rs1057521078
geneview	rs1057521078
scholar	rs1057521078
google	rs1057521078
pharmgkb	rs1057521078
gwascentral	rs1057521078
openSNP	rs1057521078
23andMe	rs1057521078
SNPshot	rs1057521078
SNPdbe	rs1057521078
MSV3d	rs1057521078
GWAS Ctlg	rs1057521078

Max Magnitude

0

ClinVar
Risk	rs1057521078(G;G)
Alt	rs1057521078(G;G)
Reference	Rs1057521078(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CHD7
CLNDBN	not provided
Reversed	0
HGVS	NC_000008.10:g.61754548A>G
CLNSRC
CLNACC	RCV000426210.1,