rs587777862

Orientation

plus

Stabilized

plus

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

Make rs587777862(C;C)

Make rs587777862(C;G)

Reference

GRCh38.p2 38.2/144

Chromosome

9

Position

128222544

Gene

DNM1

is a	snp
is	mentioned by
dbSNP	rs587777862
dbSNP (classic)	rs587777862
ClinGen	rs587777862
ebi	rs587777862
HLI	rs587777862
Exac	rs587777862
Gnomad	rs587777862
Varsome	rs587777862
LitVar	rs587777862
Map	rs587777862
PheGenI	rs587777862
Biobank	rs587777862
1000 genomes	rs587777862
hgdp	rs587777862
ensembl	rs587777862
geneview	rs587777862
scholar	rs587777862
google	rs587777862
pharmgkb	rs587777862
gwascentral	rs587777862
openSNP	rs587777862
23andMe	rs587777862
SNPshot	rs587777862
SNPdbe	rs587777862
MSV3d	rs587777862
GWAS Ctlg	rs587777862

Max Magnitude

0

ClinVar
Risk	rs587777862(C;C)
Alt	rs587777862(C;C)
Reference	Rs587777862(G;G)
Significance	Pathogenic
Disease	Epileptic encephalopathy
Variation	info
Gene	DNM1
CLNDBN	Epileptic encephalopathy, early infantile, 31
Reversed	0
HGVS	NC_000009.11:g.130984823G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000144709.7,