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

rs587777756

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587777756(-;-)
Make rs587777756(-;T)
Make rs587777756(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position32136970
GeneSPAST
is asnp
is mentioned by
dbSNPrs587777756
ebirs587777756
HLIrs587777756
Exacrs587777756
Varsomers587777756
Maprs587777756
PheGenIrs587777756
hapmaprs587777756
1000 genomesrs587777756
hgdprs587777756
ensemblrs587777756
gopubmedrs587777756
geneviewrs587777756
scholarrs587777756
googlers587777756
pharmgkbrs587777756
gwascentralrs587777756
openSNPrs587777756
23andMers587777756
23andMe allrs587777756
SNP Nexus

SNPshotrs587777756
SNPdbers587777756
MSV3drs587777756
GWAS Ctlgrs587777756
Max Magnitude0
ClinVar
Risk rs587777756(T;T)
Alt rs587777756(T;T)
Reference rs587777756(;)
Significance Pathogenic
Disease Spastic paraplegia 4
Variation info
Gene SPAST
CLNDBN Spastic paraplegia 4, autosomal dominant
Reversed 0
HGVS NC_000002.11:g.32362039dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000006021.2,