rs1057524501

Orientation

plus

Stabilized

plus

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

Make rs1057524501(A;T)

Make rs1057524501(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

60841719

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs1057524501
dbSNP (classic)	rs1057524501
ClinGen	rs1057524501
ebi	rs1057524501
HLI	rs1057524501
Exac	rs1057524501
Gnomad	rs1057524501
Varsome	rs1057524501
LitVar	rs1057524501
Map	rs1057524501
PheGenI	rs1057524501
Biobank	rs1057524501
1000 genomes	rs1057524501
hgdp	rs1057524501
ensembl	rs1057524501
geneview	rs1057524501
scholar	rs1057524501
google	rs1057524501
pharmgkb	rs1057524501
gwascentral	rs1057524501
openSNP	rs1057524501
23andMe	rs1057524501
SNPshot	rs1057524501
SNPdbe	rs1057524501
MSV3d	rs1057524501
GWAS Ctlg	rs1057524501

Max Magnitude

0

ClinVar
Risk	rs1057524501(T;T)
Alt	rs1057524501(T;T)
Reference	Rs1057524501(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CHD7
CLNDBN	not provided
Reversed	0
HGVS	NC_000008.10:g.61754278A>T
CLNSRC
CLNACC	RCV000423451.1,