rs368928190

Orientation

plus

Stabilized

plus

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

Make rs368928190(C;G)

Make rs368928190(G;G)

Reference

GRCh38.p7 38.3/149

Chromosome

16

Position

78425013

Gene

WWOX

is a	snp
is	mentioned by
dbSNP	rs368928190
dbSNP (classic)	rs368928190
ClinGen	rs368928190
ebi	rs368928190
HLI	rs368928190
Exac	rs368928190
Gnomad	rs368928190
Varsome	rs368928190
LitVar	rs368928190
Map	rs368928190
PheGenI	rs368928190
Biobank	rs368928190
1000 genomes	rs368928190
hgdp	rs368928190
ensembl	rs368928190
geneview	rs368928190
scholar	rs368928190
google	rs368928190
pharmgkb	rs368928190
gwascentral	rs368928190
openSNP	rs368928190
23andMe	rs368928190
SNPshot	rs368928190
SNPdbe	rs368928190
MSV3d	rs368928190
GWAS Ctlg	rs368928190

Max Magnitude

0

ClinVar
Risk	rs368928190(G;G) rs368928190(T;T)
Alt	rs368928190(G;G) rs368928190(T;T)
Reference	Rs368928190(C;C)
Significance	Pathogenic
Disease	Epileptic encephalopathy not provided
Variation	info
Gene	WWOX
CLNDBN	Epileptic encephalopathy, early infantile, 28 not provided
Reversed	0
HGVS	NC_000016.9:g.78458910C>G
CLNSRC
CLNACC	RCV000358651.1, RCV000413095.1,