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rs886039653

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039653(A;A)
Make rs886039653(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position78164182
GeneWWOX
is asnp
is mentioned by
dbSNPrs886039653
dbSNP (classic)rs886039653
ClinGenrs886039653
ebirs886039653
HLIrs886039653
Exacrs886039653
Gnomadrs886039653
Varsomers886039653
LitVarrs886039653
Maprs886039653
PheGenIrs886039653
Biobankrs886039653
1000 genomesrs886039653
hgdprs886039653
ensemblrs886039653
geneviewrs886039653
scholarrs886039653
googlers886039653
pharmgkbrs886039653
gwascentralrs886039653
openSNPrs886039653
23andMers886039653
23andMe allrs886039653
SNPshotrs886039653
SNPdbers886039653
MSV3drs886039653
GWAS Ctlgrs886039653
Max Magnitude0
ClinVar
Risk rs886039653(A;A)
Alt rs886039653(A;A)
Reference Rs886039653(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene WWOX
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.78198079G>A
CLNSRC
CLNACC RCV000255229.1,