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rs1064793798

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome16
Position79211666
GeneMAF, WWOX
is asnp
is mentioned by
dbSNPrs1064793798
dbSNP (old)rs1064793798
ClinGenrs1064793798
ebirs1064793798
HLIrs1064793798
Exacrs1064793798
Gnomadrs1064793798
Varsomers1064793798
Maprs1064793798
PheGenIrs1064793798
Biobankrs1064793798
1000 genomesrs1064793798
hgdprs1064793798
ensemblrs1064793798
gopubmedrs1064793798
geneviewrs1064793798
scholarrs1064793798
googlers1064793798
pharmgkbrs1064793798
gwascentralrs1064793798
openSNPrs1064793798
23andMers1064793798
23andMe allrs1064793798
SNPshotrs1064793798
SNPdbers1064793798
MSV3drs1064793798
GWAS Ctlgrs1064793798
Max Magnitude0
ClinVar
Risk rs1064793798(A;A)
Alt rs1064793798(A;A)
Reference Rs1064793798(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene WWOX
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.79245563G>A
CLNSRC
CLNACC RCV000480798.1,