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rs878854991

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878854991(A;A)
Make rs878854991(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position32141906
GeneSPAST
is asnp
is mentioned by
dbSNPrs878854991
ebirs878854991
HLIrs878854991
Exacrs878854991
Varsomers878854991
Maprs878854991
PheGenIrs878854991
hapmaprs878854991
1000 genomesrs878854991
hgdprs878854991
ensemblrs878854991
gopubmedrs878854991
geneviewrs878854991
scholarrs878854991
googlers878854991
pharmgkbrs878854991
gwascentralrs878854991
openSNPrs878854991
23andMers878854991
23andMe allrs878854991
SNP Nexus

SNPshotrs878854991
SNPdbers878854991
MSV3drs878854991
GWAS Ctlgrs878854991
Max Magnitude0
ClinVar
Risk rs878854991(A;A)
Alt rs878854991(A;A)
Reference rs878854991(G;G)
Significance Pathogenic
Disease Spastic paraplegia 4
Variation info
Gene SPAST
CLNDBN Spastic paraplegia 4, autosomal dominant
Reversed 0
HGVS NC_000002.11:g.32366975G>A
CLNSRC
CLNACC RCV000230990.1,