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rs587777752

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777752(A;G)
Make rs587777752(G;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position32147216
GeneSPAST
is asnp
is mentioned by
dbSNPrs587777752
ebirs587777752
HLIrs587777752
Exacrs587777752
Varsomers587777752
Maprs587777752
PheGenIrs587777752
hapmaprs587777752
1000 genomesrs587777752
hgdprs587777752
ensemblrs587777752
gopubmedrs587777752
geneviewrs587777752
scholarrs587777752
googlers587777752
pharmgkbrs587777752
gwascentralrs587777752
openSNPrs587777752
23andMers587777752
23andMe allrs587777752
SNP Nexus

SNPshotrs587777752
SNPdbers587777752
MSV3drs587777752
GWAS Ctlgrs587777752
Max Magnitude0
ClinVar
Risk rs587777752(G;G)
Alt rs587777752(G;G)
Reference rs587777752(A;A)
Significance Pathogenic
Disease Spastic paraplegia 4
Variation info
Gene SPAST
CLNDBN Spastic paraplegia 4, autosomal dominant
Reversed 0
HGVS NC_000002.11:g.32372285A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000006015.2,