rs1057517956

Orientation

plus

Stabilized

plus

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

Make rs1057517956(G;T)

Make rs1057517956(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

60853482

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs1057517956
dbSNP (classic)	rs1057517956
ClinGen	rs1057517956
ebi	rs1057517956
HLI	rs1057517956
Exac	rs1057517956
Gnomad	rs1057517956
Varsome	rs1057517956
LitVar	rs1057517956
Map	rs1057517956
PheGenI	rs1057517956
Biobank	rs1057517956
1000 genomes	rs1057517956
hgdp	rs1057517956
ensembl	rs1057517956
geneview	rs1057517956
scholar	rs1057517956
google	rs1057517956
pharmgkb	rs1057517956
gwascentral	rs1057517956
openSNP	rs1057517956
23andMe	rs1057517956
SNPshot	rs1057517956
SNPdbe	rs1057517956
MSV3d	rs1057517956
GWAS Ctlg	rs1057517956

Max Magnitude

0

ClinVar
Risk	rs1057517956(T;T)
Alt	rs1057517956(T;T)
Reference	Rs1057517956(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CHD7
CLNDBN	not provided
Reversed	0
HGVS	NC_000008.10:g.61766041G>T
CLNSRC
CLNACC	RCV000412832.1,