rs991738444

Orientation

plus

Stabilized

plus

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

Make rs991738444(A;A)

Make rs991738444(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

14

Position

21400569

Gene

CHD8

is a	snp
is	mentioned by
dbSNP	rs991738444
dbSNP (classic)	rs991738444
ClinGen	rs991738444
ebi	rs991738444
HLI	rs991738444
Exac	rs991738444
Gnomad	rs991738444
Varsome	rs991738444
LitVar	rs991738444
Map	rs991738444
PheGenI	rs991738444
Biobank	rs991738444
1000 genomes	rs991738444
hgdp	rs991738444
ensembl	rs991738444
geneview	rs991738444
scholar	rs991738444
google	rs991738444
pharmgkb	rs991738444
gwascentral	rs991738444
openSNP	rs991738444
23andMe	rs991738444
SNPshot	rs991738444
SNPdbe	rs991738444
MSV3d	rs991738444
GWAS Ctlg	rs991738444

Max Magnitude

0

ClinVar
Risk	rs991738444(A;A) rs991738444(T;T)
Alt	rs991738444(A;A) rs991738444(T;T)
Reference	Rs991738444(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene
CLNDBN	not provided
Reversed	0
HGVS	NC_000014.8:g.21868728G>A
CLNSRC
CLNACC	RCV000482586.1,