rs1057518128

Orientation

plus

Stabilized

plus

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

Make rs1057518128(C;T)

Make rs1057518128(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

92927289

Gene

CHD2

is a	snp
is	mentioned by
dbSNP	rs1057518128
dbSNP (classic)	rs1057518128
ClinGen	rs1057518128
ebi	rs1057518128
HLI	rs1057518128
Exac	rs1057518128
Gnomad	rs1057518128
Varsome	rs1057518128
LitVar	rs1057518128
Map	rs1057518128
PheGenI	rs1057518128
Biobank	rs1057518128
1000 genomes	rs1057518128
hgdp	rs1057518128
ensembl	rs1057518128
geneview	rs1057518128
scholar	rs1057518128
google	rs1057518128
pharmgkb	rs1057518128
gwascentral	rs1057518128
openSNP	rs1057518128
23andMe	rs1057518128
SNPshot	rs1057518128
SNPdbe	rs1057518128
MSV3d	rs1057518128
GWAS Ctlg	rs1057518128

Max Magnitude

0

ClinVar
Risk	rs1057518128(T;T)
Alt	rs1057518128(T;T)
Reference	Rs1057518128(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CHD2
CLNDBN	not provided
Reversed	0
HGVS	NC_000015.9:g.93470519C>T
CLNSRC
CLNACC	RCV000413171.1,