rs730880292

Orientation

plus

Stabilized

plus

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

Make rs730880292(C;G)

Make rs730880292(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

16

Position

78108455

Gene

WWOX

is a	snp
is	mentioned by
dbSNP	rs730880292
dbSNP (classic)	rs730880292
ClinGen	rs730880292
ebi	rs730880292
HLI	rs730880292
Exac	rs730880292
Gnomad	rs730880292
Varsome	rs730880292
LitVar	rs730880292
Map	rs730880292
PheGenI	rs730880292
Biobank	rs730880292
1000 genomes	rs730880292
hgdp	rs730880292
ensembl	rs730880292
geneview	rs730880292
scholar	rs730880292
google	rs730880292
pharmgkb	rs730880292
gwascentral	rs730880292
openSNP	rs730880292
23andMe	rs730880292
SNPshot	rs730880292
SNPdbe	rs730880292
MSV3d	rs730880292
GWAS Ctlg	rs730880292

Max Magnitude

0

ClinVar
Risk	rs730880292(G;G)
Alt	rs730880292(G;G)
Reference	Rs730880292(C;C)
Significance	Pathogenic
Disease	Epileptic encephalopathy
Variation	info
Gene	WWOX
CLNDBN	Epileptic encephalopathy, early infantile, 28
Reversed	0
HGVS	NC_000016.9:g.78142352C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000157088.3,