rs1057521077

Orientation

plus

Stabilized

plus

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

Make rs1057521077(C;C)

Make rs1057521077(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

60822604

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs1057521077
dbSNP (classic)	rs1057521077
ClinGen	rs1057521077
ebi	rs1057521077
HLI	rs1057521077
Exac	rs1057521077
Gnomad	rs1057521077
Varsome	rs1057521077
LitVar	rs1057521077
Map	rs1057521077
PheGenI	rs1057521077
Biobank	rs1057521077
1000 genomes	rs1057521077
hgdp	rs1057521077
ensembl	rs1057521077
geneview	rs1057521077
scholar	rs1057521077
google	rs1057521077
pharmgkb	rs1057521077
gwascentral	rs1057521077
openSNP	rs1057521077
23andMe	rs1057521077
SNPshot	rs1057521077
SNPdbe	rs1057521077
MSV3d	rs1057521077
GWAS Ctlg	rs1057521077

Max Magnitude

0

ClinVar
Risk	rs1057521077(C;C)
Alt	rs1057521077(C;C)
Reference	Rs1057521077(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CHD7
CLNDBN	not provided
Reversed	0
HGVS	NC_000008.10:g.61735163T>C
CLNSRC
CLNACC	RCV000445135.1,