rs1057520592

Orientation

plus

Stabilized

plus

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

Make rs1057520592(A;A)

Make rs1057520592(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

92955513

Gene

CHD2

is a	snp
is	mentioned by
dbSNP	rs1057520592
dbSNP (classic)	rs1057520592
ClinGen	rs1057520592
ebi	rs1057520592
HLI	rs1057520592
Exac	rs1057520592
Gnomad	rs1057520592
Varsome	rs1057520592
LitVar	rs1057520592
Map	rs1057520592
PheGenI	rs1057520592
Biobank	rs1057520592
1000 genomes	rs1057520592
hgdp	rs1057520592
ensembl	rs1057520592
geneview	rs1057520592
scholar	rs1057520592
google	rs1057520592
pharmgkb	rs1057520592
gwascentral	rs1057520592
openSNP	rs1057520592
23andMe	rs1057520592
SNPshot	rs1057520592
SNPdbe	rs1057520592
MSV3d	rs1057520592
GWAS Ctlg	rs1057520592

Max Magnitude

0

ClinVar
Risk	rs1057520592(A;A)
Alt	rs1057520592(A;A)
Reference	Rs1057520592(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CHD2
CLNDBN	not provided
Reversed	0
HGVS	NC_000015.9:g.93498743G>A
CLNSRC
CLNACC	RCV000426945.1,