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rs864622179

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864622179(A;A)
Make rs864622179(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position32144996
GeneSPAST
is asnp
is mentioned by
dbSNPrs864622179
ebirs864622179
HLIrs864622179
Exacrs864622179
Varsomers864622179
Maprs864622179
PheGenIrs864622179
hapmaprs864622179
1000 genomesrs864622179
hgdprs864622179
ensemblrs864622179
gopubmedrs864622179
geneviewrs864622179
scholarrs864622179
googlers864622179
pharmgkbrs864622179
gwascentralrs864622179
openSNPrs864622179
23andMers864622179
23andMe allrs864622179
SNP Nexus

SNPshotrs864622179
SNPdbers864622179
MSV3drs864622179
GWAS Ctlgrs864622179
Max Magnitude0
ClinVar
Risk rs864622179(A;A)
Alt rs864622179(A;A)
Reference Rs864622179(G;G)
Significance Probable-Pathogenic
Disease Spastic paraplegia 4
Variation info
Gene SPAST
CLNDBN Spastic paraplegia 4, autosomal dominant
Reversed 0
HGVS NC_000002.11:g.32370065G>A
CLNSRC
CLNACC RCV000205236.2,