rs1057524339

Orientation

minus

Stabilized

minus

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

Make rs1057524339(A;G)

Make rs1057524339(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

14

Position

21408557

Gene

CHD8

is a	snp
is	mentioned by
dbSNP	rs1057524339
dbSNP (classic)	rs1057524339
ClinGen	rs1057524339
ebi	rs1057524339
HLI	rs1057524339
Exac	rs1057524339
Gnomad	rs1057524339
Varsome	rs1057524339
LitVar	rs1057524339
Map	rs1057524339
PheGenI	rs1057524339
Biobank	rs1057524339
1000 genomes	rs1057524339
hgdp	rs1057524339
ensembl	rs1057524339
geneview	rs1057524339
scholar	rs1057524339
google	rs1057524339
pharmgkb	rs1057524339
gwascentral	rs1057524339
openSNP	rs1057524339
23andMe	rs1057524339
SNPshot	rs1057524339
SNPdbe	rs1057524339
MSV3d	rs1057524339
GWAS Ctlg	rs1057524339

Max Magnitude

0

ClinVar
Risk	rs1057524339(G;G)
Alt	rs1057524339(G;G)
Reference	Rs1057524339(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CHD8
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.21876716T>C
CLNSRC
CLNACC	RCV000423157.1,