rs1057520712

Orientation

plus

Stabilized

plus

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

Make rs1057520712(G;T)

Make rs1057520712(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

60852900

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs1057520712
dbSNP (classic)	rs1057520712
ClinGen	rs1057520712
ebi	rs1057520712
HLI	rs1057520712
Exac	rs1057520712
Gnomad	rs1057520712
Varsome	rs1057520712
LitVar	rs1057520712
Map	rs1057520712
PheGenI	rs1057520712
Biobank	rs1057520712
1000 genomes	rs1057520712
hgdp	rs1057520712
ensembl	rs1057520712
geneview	rs1057520712
scholar	rs1057520712
google	rs1057520712
pharmgkb	rs1057520712
gwascentral	rs1057520712
openSNP	rs1057520712
23andMe	rs1057520712
SNPshot	rs1057520712
SNPdbe	rs1057520712
MSV3d	rs1057520712
GWAS Ctlg	rs1057520712

Max Magnitude

0

ClinVar
Risk	rs1057520712(T;T)
Alt	rs1057520712(T;T)
Reference	Rs1057520712(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CHD7
CLNDBN	not provided
Reversed	0
HGVS	NC_000008.10:g.61765459G>T
CLNSRC
CLNACC	RCV000438702.1,