rs119487098

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common in complete genomics

Make rs119487098(C;C)

Make rs119487098(C;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

78432568

Gene

WWOX

is a	snp
is	mentioned by
dbSNP	rs119487098
dbSNP (classic)	rs119487098
ClinGen	rs119487098
ebi	rs119487098
HLI	rs119487098
Exac	rs119487098
Gnomad	rs119487098
Varsome	rs119487098
LitVar	rs119487098
Map	rs119487098
PheGenI	rs119487098
Biobank	rs119487098
1000 genomes	rs119487098
hgdp	rs119487098
ensembl	rs119487098
geneview	rs119487098
scholar	rs119487098
google	rs119487098
pharmgkb	rs119487098
gwascentral	rs119487098
openSNP	rs119487098
23andMe	rs119487098
SNPshot	rs119487098
SNPdbe	rs119487098
MSV3d	rs119487098
GWAS Ctlg	rs119487098

Max Magnitude

0

OMIM	605131
Desc
Variant	0001
Related	also

ClinVar
Risk	rs119487098(C;C)
Alt	rs119487098(C;C)
Reference	Rs119487098(T;T)
Significance	Pathogenic
Disease	Esophageal squamous cell carcinoma
Variation	info
Gene	WWOX
CLNDBN	Esophageal squamous cell carcinoma, somatic
Reversed	0
HGVS	NC_000016.9:g.78466465T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005513.4,