rs1057519228

Orientation

plus

Stabilized

plus

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

Make rs1057519228(A;A)

Make rs1057519228(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

92953573

Gene

CHD2

is a	snp
is	mentioned by
dbSNP	rs1057519228
dbSNP (classic)	rs1057519228
ClinGen	rs1057519228
ebi	rs1057519228
HLI	rs1057519228
Exac	rs1057519228
Gnomad	rs1057519228
Varsome	rs1057519228
LitVar	rs1057519228
Map	rs1057519228
PheGenI	rs1057519228
Biobank	rs1057519228
1000 genomes	rs1057519228
hgdp	rs1057519228
ensembl	rs1057519228
geneview	rs1057519228
scholar	rs1057519228
google	rs1057519228
pharmgkb	rs1057519228
gwascentral	rs1057519228
openSNP	rs1057519228
23andMe	rs1057519228
SNPshot	rs1057519228
SNPdbe	rs1057519228
MSV3d	rs1057519228
GWAS Ctlg	rs1057519228

Max Magnitude

0

ClinVar
Risk	rs1057519228(A;A)
Alt	rs1057519228(A;A)
Reference	Rs1057519228(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CHD2
CLNDBN	not provided
Reversed	0
HGVS	NC_000015.9:g.93496803G>A
CLNSRC
CLNACC	RCV000415729.1,