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rs121908517

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908517(A;A)
Make rs121908517(A;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position32063965
GeneHP11026, SPAST
is asnp
is mentioned by
dbSNPrs121908517
ebirs121908517
HLIrs121908517
Exacrs121908517
Varsomers121908517
Maprs121908517
PheGenIrs121908517
hapmaprs121908517
1000 genomesrs121908517
hgdprs121908517
ensemblrs121908517
gopubmedrs121908517
geneviewrs121908517
scholarrs121908517
googlers121908517
pharmgkbrs121908517
gwascentralrs121908517
openSNPrs121908517
23andMers121908517
23andMe allrs121908517
SNP Nexus

SNPshotrs121908517
SNPdbers121908517
MSV3drs121908517
GWAS Ctlgrs121908517
Max Magnitude0
OMIM604277
Desc
Variant0017
Relatedalso
ClinVar
Risk rs121908517(A;A)
Alt rs121908517(A;A)
Reference rs121908517(C;C)
Significance Other
Disease Spastic paraplegia 4
Variation info
Gene SPAST
CLNDBN Spastic paraplegia 4, modifier of
Reversed 0
HGVS NC_000002.11:g.32289034C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006026.3,