rs1057517957

Orientation

plus

Stabilized

plus

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

Make rs1057517957(-;C)

Make rs1057517957(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

60860950

Gene

CHD7

is a	snp
is	mentioned by
dbSNP	rs1057517957
dbSNP (classic)	rs1057517957
ClinGen	rs1057517957
ebi	rs1057517957
HLI	rs1057517957
Exac	rs1057517957
Gnomad	rs1057517957
Varsome	rs1057517957
LitVar	rs1057517957
Map	rs1057517957
PheGenI	rs1057517957
Biobank	rs1057517957
1000 genomes	rs1057517957
hgdp	rs1057517957
ensembl	rs1057517957
geneview	rs1057517957
scholar	rs1057517957
google	rs1057517957
pharmgkb	rs1057517957
gwascentral	rs1057517957
openSNP	rs1057517957
23andMe	rs1057517957
SNPshot	rs1057517957
SNPdbe	rs1057517957
MSV3d	rs1057517957
GWAS Ctlg	rs1057517957

Max Magnitude

0

ClinVar
Risk	rs1057517957(C;C)
Alt	rs1057517957(C;C)
Reference	Rs1057517957(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CHD7
CLNDBN	not provided
Reversed	0
HGVS	NC_000008.10:g.61773509dupC
CLNSRC
CLNACC	RCV000413712.1,