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rs878854990

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878854990(C;T)
Make rs878854990(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position32136933
GeneSPAST
is asnp
is mentioned by
dbSNPrs878854990
ebirs878854990
HLIrs878854990
Exacrs878854990
Varsomers878854990
Maprs878854990
PheGenIrs878854990
hapmaprs878854990
1000 genomesrs878854990
hgdprs878854990
ensemblrs878854990
gopubmedrs878854990
geneviewrs878854990
scholarrs878854990
googlers878854990
pharmgkbrs878854990
gwascentralrs878854990
openSNPrs878854990
23andMers878854990
23andMe allrs878854990
SNP Nexus

SNPshotrs878854990
SNPdbers878854990
MSV3drs878854990
GWAS Ctlgrs878854990
Max Magnitude0
ClinVar
Risk rs878854990(T;T)
Alt rs878854990(T;T)
Reference rs878854990(C;C)
Significance Pathogenic
Disease Spastic paraplegia 4
Variation info
Gene SPAST
CLNDBN Spastic paraplegia 4, autosomal dominant
Reversed 0
HGVS NC_000002.11:g.32362002C>T
CLNSRC
CLNACC RCV000234461.1,