rs1057523712

Orientation

minus

Stabilized

minus

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

Make rs1057523712(C;C)

Make rs1057523712(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

14

Position

21402055

Gene

CHD8

is a	snp
is	mentioned by
dbSNP	rs1057523712
dbSNP (classic)	rs1057523712
ClinGen	rs1057523712
ebi	rs1057523712
HLI	rs1057523712
Exac	rs1057523712
Gnomad	rs1057523712
Varsome	rs1057523712
LitVar	rs1057523712
Map	rs1057523712
PheGenI	rs1057523712
Biobank	rs1057523712
1000 genomes	rs1057523712
hgdp	rs1057523712
ensembl	rs1057523712
geneview	rs1057523712
scholar	rs1057523712
google	rs1057523712
pharmgkb	rs1057523712
gwascentral	rs1057523712
openSNP	rs1057523712
23andMe	rs1057523712
SNPshot	rs1057523712
SNPdbe	rs1057523712
MSV3d	rs1057523712
GWAS Ctlg	rs1057523712

Max Magnitude

0

ClinVar
Risk	rs1057523712(C;C)
Alt	rs1057523712(C;C)
Reference	Rs1057523712(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CHD8
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.21870214C>G
CLNSRC
CLNACC	RCV000432820.1,