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rs121908510

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908510(A;A)
Make rs121908510(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position32136898
GeneSPAST
is asnp
is mentioned by
dbSNPrs121908510
ebirs121908510
HLIrs121908510
Exacrs121908510
Varsomers121908510
Maprs121908510
PheGenIrs121908510
hapmaprs121908510
1000 genomesrs121908510
hgdprs121908510
ensemblrs121908510
gopubmedrs121908510
geneviewrs121908510
scholarrs121908510
googlers121908510
pharmgkbrs121908510
gwascentralrs121908510
openSNPrs121908510
23andMers121908510
23andMe allrs121908510
SNP Nexus

SNPshotrs121908510
SNPdbers121908510
MSV3drs121908510
GWAS Ctlgrs121908510
Max Magnitude0
OMIM604277
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121908510(A;A)
Alt rs121908510(A;A)
Reference rs121908510(G;G)
Significance Pathogenic
Disease Spastic paraplegia 4
Variation info
Gene SPAST
CLNDBN Spastic paraplegia 4, autosomal dominant
Reversed 0
HGVS NC_000002.11:g.32361967G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006012.2,