rs864309544

Orientation

plus

Stabilized

plus

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

Make rs864309544(-;-)

Make rs864309544(-;AGTCAAAAGATAAGAAAGA)

Make rs864309544(AGTCAAAAGATAAGAAAGA;AGTCAAAAGATAAGAAAGA)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

93002295

Gene

CHD2

is a	snp
is	mentioned by
dbSNP	rs864309544
dbSNP (classic)	rs864309544
ClinGen	rs864309544
ebi	rs864309544
HLI	rs864309544
Exac	rs864309544
Gnomad	rs864309544
Varsome	rs864309544
LitVar	rs864309544
Map	rs864309544
PheGenI	rs864309544
Biobank	rs864309544
1000 genomes	rs864309544
hgdp	rs864309544
ensembl	rs864309544
geneview	rs864309544
scholar	rs864309544
google	rs864309544
pharmgkb	rs864309544
gwascentral	rs864309544
openSNP	rs864309544
23andMe	rs864309544
SNPshot	rs864309544
SNPdbe	rs864309544
MSV3d	rs864309544
GWAS Ctlg	rs864309544

Max Magnitude

0

ClinVar
Risk	rs864309544(-;-)
Alt	rs864309544(-;-)
Reference	Rs864309544(AAGAAAGAAGTCAAAAGAT;AAGAAAGAAGTCAAAAGAT)
Significance	Pathogenic
Disease	Epileptic encephalopathy
Variation	info
Gene	CHD2
CLNDBN	Epileptic encephalopathy, childhood-onset
Reversed	0
HGVS	NC_000015.9:g.93545525_93545543del19
CLNSRC
CLNACC	RCV000202639.1,