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rs9929635

From SNPedia

Orientationplus
Stabilizedplus
Make rs9929635(A;A)
Make rs9929635(A;T)
Make rs9929635(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position79066662
GeneWWOX
is asnp
is mentioned by
dbSNPrs9929635
ebirs9929635
HLIrs9929635
Exacrs9929635
Varsomers9929635
Maprs9929635
PheGenIrs9929635
hapmaprs9929635
1000 genomesrs9929635
hgdprs9929635
ensemblrs9929635
gopubmedrs9929635
geneviewrs9929635
scholarrs9929635
googlers9929635
pharmgkbrs9929635
gwascentralrs9929635
openSNPrs9929635
23andMers9929635
23andMe allrs9929635
SNP Nexus

SNPshotrs9929635
SNPdbers9929635
MSV3drs9929635
GWAS Ctlgrs9929635
GMAF0.2709
Max Magnitude
? (A;A) (A;T) (T;T) 28
OMIM612319
DescSPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE; SPG35
Variant
Relatedalso

[PMID 18463364] A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23.