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rs878854992

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878854992(C;C)
Make rs878854992(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position32144995
GeneSPAST
is asnp
is mentioned by
dbSNPrs878854992
ebirs878854992
HLIrs878854992
Exacrs878854992
Varsomers878854992
Maprs878854992
PheGenIrs878854992
hapmaprs878854992
1000 genomesrs878854992
hgdprs878854992
ensemblrs878854992
gopubmedrs878854992
geneviewrs878854992
scholarrs878854992
googlers878854992
pharmgkbrs878854992
gwascentralrs878854992
openSNPrs878854992
23andMers878854992
23andMe allrs878854992
SNP Nexus

SNPshotrs878854992
SNPdbers878854992
MSV3drs878854992
GWAS Ctlgrs878854992
Max Magnitude0
ClinVar
Risk rs878854992(C;C)
Alt rs878854992(C;C)
Reference rs878854992(G;G)
Significance Probable-Pathogenic
Disease Spastic paraplegia 4
Variation info
Gene SPAST
CLNDBN Spastic paraplegia 4, autosomal dominant
Reversed 0
HGVS NC_000002.11:g.32370064G>C
CLNSRC
CLNACC RCV000228683.1,