rs1057519563

Orientation

minus

Stabilized

minus

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

Make rs1057519563(C;T)

Make rs1057519563(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

9160835

Gene

DENND5A

is a	snp
is	mentioned by
dbSNP	rs1057519563
dbSNP (classic)	rs1057519563
ClinGen	rs1057519563
ebi	rs1057519563
HLI	rs1057519563
Exac	rs1057519563
Gnomad	rs1057519563
Varsome	rs1057519563
LitVar	rs1057519563
Map	rs1057519563
PheGenI	rs1057519563
Biobank	rs1057519563
1000 genomes	rs1057519563
hgdp	rs1057519563
ensembl	rs1057519563
geneview	rs1057519563
scholar	rs1057519563
google	rs1057519563
pharmgkb	rs1057519563
gwascentral	rs1057519563
openSNP	rs1057519563
23andMe	rs1057519563
SNPshot	rs1057519563
SNPdbe	rs1057519563
MSV3d	rs1057519563
GWAS Ctlg	rs1057519563

Max Magnitude

0

ClinVar
Risk	rs1057519563(T;T)
Alt	rs1057519563(T;T)
Reference	Rs1057519563(C;C)
Significance	Probable-Pathogenic
Disease	Epileptic encephalopathy
Variation	info
Gene	DENND5A
CLNDBN	Epileptic encephalopathy, early infantile, 49
Reversed	1
HGVS	NC_000011.9:g.9182382G>A
CLNSRC
CLNACC	RCV000416961.1,