rs1057524677

Orientation

minus

Stabilized

minus

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

Make rs1057524677(C;T)

Make rs1057524677(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

14

Position

21426154

Gene

CHD8

is a	snp
is	mentioned by
dbSNP	rs1057524677
dbSNP (classic)	rs1057524677
ClinGen	rs1057524677
ebi	rs1057524677
HLI	rs1057524677
Exac	rs1057524677
Gnomad	rs1057524677
Varsome	rs1057524677
LitVar	rs1057524677
Map	rs1057524677
PheGenI	rs1057524677
Biobank	rs1057524677
1000 genomes	rs1057524677
hgdp	rs1057524677
ensembl	rs1057524677
geneview	rs1057524677
scholar	rs1057524677
google	rs1057524677
pharmgkb	rs1057524677
gwascentral	rs1057524677
openSNP	rs1057524677
23andMe	rs1057524677
SNPshot	rs1057524677
SNPdbe	rs1057524677
MSV3d	rs1057524677
GWAS Ctlg	rs1057524677

Max Magnitude

0

ClinVar
Risk	rs1057524677(T;T)
Alt	rs1057524677(T;T)
Reference	Rs1057524677(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CHD8
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.21894313G>A
CLNSRC
CLNACC	RCV000440969.1,