rs759766243

Orientation

plus

Stabilized

plus

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

Make rs759766243(C;T)

Make rs759766243(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

78109788

Gene

WWOX

is a	snp
is	mentioned by
dbSNP	rs759766243
dbSNP (classic)	rs759766243
ClinGen	rs759766243
ebi	rs759766243
HLI	rs759766243
Exac	rs759766243
Gnomad	rs759766243
Varsome	rs759766243
LitVar	rs759766243
Map	rs759766243
PheGenI	rs759766243
Biobank	rs759766243
1000 genomes	rs759766243
hgdp	rs759766243
ensembl	rs759766243
geneview	rs759766243
scholar	rs759766243
google	rs759766243
pharmgkb	rs759766243
gwascentral	rs759766243
openSNP	rs759766243
23andMe	rs759766243
SNPshot	rs759766243
SNPdbe	rs759766243
MSV3d	rs759766243
GWAS Ctlg	rs759766243

Max Magnitude

0

ClinVar
Risk	rs759766243(A;A) rs759766243(T;T)
Alt	rs759766243(A;A) rs759766243(T;T)
Reference	Rs759766243(C;C)
Significance	Probable-Pathogenic
Disease	Epileptic encephalopathy
Variation	info
Gene	WWOX
CLNDBN	Epileptic encephalopathy
Reversed	0
HGVS	NC_000016.9:g.78143685C>A
CLNSRC
CLNACC	RCV000415297.1,