Have questions? Visit https://www.reddit.com/r/SNPedia

rs587777753

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587777753(-;-)
Make rs587777753(-;A)
Make rs587777753(A;A)
ReferenceGRCh38 38.1/142
Chromosome2
Position32087529
GeneSPAST
is asnp
is mentioned by
dbSNPrs587777753
ebirs587777753
HLIrs587777753
Exacrs587777753
Varsomers587777753
Maprs587777753
PheGenIrs587777753
hapmaprs587777753
1000 genomesrs587777753
hgdprs587777753
ensemblrs587777753
gopubmedrs587777753
geneviewrs587777753
scholarrs587777753
googlers587777753
pharmgkbrs587777753
gwascentralrs587777753
openSNPrs587777753
23andMers587777753
23andMe allrs587777753
SNP Nexus

SNPshotrs587777753
SNPdbers587777753
MSV3drs587777753
GWAS Ctlgrs587777753
Max Magnitude0
ClinVar
Risk rs587777753(A;A)
Alt rs587777753(A;A)
Reference rs587777753(;)
Significance Pathogenic
Disease Spastic paraplegia 4
Variation info
Gene SPAST
CLNDBN Spastic paraplegia 4, autosomal dominant
Reversed 0
HGVS NC_000002.11:g.32312598dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000006017.2,