rs1057520734

Orientation

plus

Stabilized

plus

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

Make rs1057520734(C;T)

Make rs1057520734(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

60742555

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs1057520734
dbSNP (classic)	rs1057520734
ClinGen	rs1057520734
ebi	rs1057520734
HLI	rs1057520734
Exac	rs1057520734
Gnomad	rs1057520734
Varsome	rs1057520734
LitVar	rs1057520734
Map	rs1057520734
PheGenI	rs1057520734
Biobank	rs1057520734
1000 genomes	rs1057520734
hgdp	rs1057520734
ensembl	rs1057520734
geneview	rs1057520734
scholar	rs1057520734
google	rs1057520734
pharmgkb	rs1057520734
gwascentral	rs1057520734
openSNP	rs1057520734
23andMe	rs1057520734
SNPshot	rs1057520734
SNPdbe	rs1057520734
MSV3d	rs1057520734
GWAS Ctlg	rs1057520734

Max Magnitude

0

ClinVar
Risk	rs1057520734(T;T)
Alt	rs1057520734(T;T)
Reference	Rs1057520734(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CHD7
CLNDBN	not provided
Reversed	0
HGVS	NC_000008.10:g.61655114C>T
CLNSRC
CLNACC	RCV000441742.1,