rs1057518236

Orientation

plus

Stabilized

plus

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

Make rs1057518236(C;T)

Make rs1057518236(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

92949036

Gene

CHD2

is a	snp
is	mentioned by
dbSNP	rs1057518236
dbSNP (classic)	rs1057518236
ClinGen	rs1057518236
ebi	rs1057518236
HLI	rs1057518236
Exac	rs1057518236
Gnomad	rs1057518236
Varsome	rs1057518236
LitVar	rs1057518236
Map	rs1057518236
PheGenI	rs1057518236
Biobank	rs1057518236
1000 genomes	rs1057518236
hgdp	rs1057518236
ensembl	rs1057518236
geneview	rs1057518236
scholar	rs1057518236
google	rs1057518236
pharmgkb	rs1057518236
gwascentral	rs1057518236
openSNP	rs1057518236
23andMe	rs1057518236
SNPshot	rs1057518236
SNPdbe	rs1057518236
MSV3d	rs1057518236
GWAS Ctlg	rs1057518236

Max Magnitude

0

ClinVar
Risk	rs1057518236(T;T)
Alt	rs1057518236(T;T)
Reference	Rs1057518236(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CHD2
CLNDBN	not provided
Reversed	0
HGVS	NC_000015.9:g.93492266C>T
CLNSRC
CLNACC	RCV000413801.1,