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rs587777755

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777755(A;G)
Make rs587777755(G;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position32128483
GeneSPAST
is asnp
is mentioned by
dbSNPrs587777755
ebirs587777755
HLIrs587777755
Exacrs587777755
Varsomers587777755
Maprs587777755
PheGenIrs587777755
hapmaprs587777755
1000 genomesrs587777755
hgdprs587777755
ensemblrs587777755
gopubmedrs587777755
geneviewrs587777755
scholarrs587777755
googlers587777755
pharmgkbrs587777755
gwascentralrs587777755
openSNPrs587777755
23andMers587777755
23andMe allrs587777755
SNP Nexus

SNPshotrs587777755
SNPdbers587777755
MSV3drs587777755
GWAS Ctlgrs587777755
Max Magnitude0
ClinVar
Risk rs587777755(G;G)
Alt rs587777755(G;G)
Reference rs587777755(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.32353552A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000006020.2,