rs878855021

Orientation

plus

Stabilized

plus

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

Make rs878855021(C;G)

Make rs878855021(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

78425043

Gene

WWOX

is a	snp
is	mentioned by
dbSNP	rs878855021
dbSNP (classic)	rs878855021
ClinGen	rs878855021
ebi	rs878855021
HLI	rs878855021
Exac	rs878855021
Gnomad	rs878855021
Varsome	rs878855021
LitVar	rs878855021
Map	rs878855021
PheGenI	rs878855021
Biobank	rs878855021
1000 genomes	rs878855021
hgdp	rs878855021
ensembl	rs878855021
geneview	rs878855021
scholar	rs878855021
google	rs878855021
pharmgkb	rs878855021
gwascentral	rs878855021
openSNP	rs878855021
23andMe	rs878855021
SNPshot	rs878855021
SNPdbe	rs878855021
MSV3d	rs878855021
GWAS Ctlg	rs878855021

Max Magnitude

0

ClinVar
Risk	rs878855021(G;G)
Alt	rs878855021(G;G)
Reference	Rs878855021(C;C)
Significance	Pathogenic
Disease	Epileptic encephalopathy Spinocerebellar ataxia
Variation	info
Gene	WWOX
CLNDBN	Epileptic encephalopathy, early infantile, 1 Spinocerebellar ataxia, autosomal recessive 12
Reversed	0
HGVS	NC_000016.9:g.78458940C>G
CLNSRC
CLNACC	RCV000234306.2,