rs9929635
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9929635(A;A) |
Make rs9929635(A;T) |
Make rs9929635(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 79066662 |
Gene | WWOX |
is a | snp |
is | mentioned by |
dbSNP | rs9929635 |
dbSNP (classic) | rs9929635 |
ClinGen | rs9929635 |
ebi | rs9929635 |
HLI | rs9929635 |
Exac | rs9929635 |
Gnomad | rs9929635 |
Varsome | rs9929635 |
LitVar | rs9929635 |
Map | rs9929635 |
PheGenI | rs9929635 |
Biobank | rs9929635 |
1000 genomes | rs9929635 |
hgdp | rs9929635 |
ensembl | rs9929635 |
geneview | rs9929635 |
scholar | rs9929635 |
rs9929635 | |
pharmgkb | rs9929635 |
gwascentral | rs9929635 |
openSNP | rs9929635 |
23andMe | rs9929635 |
SNPshot | rs9929635 |
SNPdbe | rs9929635 |
MSV3d | rs9929635 |
GWAS Ctlg | rs9929635 |
GMAF | 0.2709 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 18463364] A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23.