rs1060502727

Orientation

plus

Stabilized

plus

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

Make rs1060502727(C;C)

Make rs1060502727(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

78115155

Gene

WWOX

is a	snp
is	mentioned by
dbSNP	rs1060502727
dbSNP (classic)	rs1060502727
ClinGen	rs1060502727
ebi	rs1060502727
HLI	rs1060502727
Exac	rs1060502727
Gnomad	rs1060502727
Varsome	rs1060502727
LitVar	rs1060502727
Map	rs1060502727
PheGenI	rs1060502727
Biobank	rs1060502727
1000 genomes	rs1060502727
hgdp	rs1060502727
ensembl	rs1060502727
geneview	rs1060502727
scholar	rs1060502727
google	rs1060502727
pharmgkb	rs1060502727
gwascentral	rs1060502727
openSNP	rs1060502727
23andMe	rs1060502727
SNPshot	rs1060502727
SNPdbe	rs1060502727
MSV3d	rs1060502727
GWAS Ctlg	rs1060502727

Max Magnitude

0

ClinVar
Risk	rs1060502727(C;C)
Alt	rs1060502727(C;C)
Reference	Rs1060502727(G;G)
Significance	Probable-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.78149052G>C
CLNSRC
CLNACC	RCV000458905.1,