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rs990150249

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position78115000
GeneWWOX
is asnp
is mentioned by
dbSNPrs990150249
dbSNP (classic)rs990150249
ClinGenrs990150249
ebirs990150249
HLIrs990150249
Exacrs990150249
Gnomadrs990150249
Varsomers990150249
LitVarrs990150249
Maprs990150249
PheGenIrs990150249
Biobankrs990150249
1000 genomesrs990150249
hgdprs990150249
ensemblrs990150249
geneviewrs990150249
scholarrs990150249
googlers990150249
pharmgkbrs990150249
gwascentralrs990150249
openSNPrs990150249
23andMers990150249
23andMe allrs990150249
SNPshotrs990150249
SNPdbers990150249
MSV3drs990150249
GWAS Ctlgrs990150249
Max Magnitude0
ClinVar
Risk rs990150249(G;G)
Alt rs990150249(G;G)
Reference Rs990150249(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.78148897C>G
CLNSRC
CLNACC RCV000487411.1,