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rs875989878

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs875989878(A;A)
Make rs875989878(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position32128480
GeneSPAST
is asnp
is mentioned by
dbSNPrs875989878
ebirs875989878
HLIrs875989878
Exacrs875989878
Varsomers875989878
Maprs875989878
PheGenIrs875989878
hapmaprs875989878
1000 genomesrs875989878
hgdprs875989878
ensemblrs875989878
gopubmedrs875989878
geneviewrs875989878
scholarrs875989878
googlers875989878
pharmgkbrs875989878
gwascentralrs875989878
openSNPrs875989878
23andMers875989878
23andMe allrs875989878
SNP Nexus

SNPshotrs875989878
SNPdbers875989878
MSV3drs875989878
GWAS Ctlgrs875989878
Max Magnitude0
ClinVar
Risk rs875989878(A;A)
Alt rs875989878(A;A)
Reference rs875989878(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.32353549G>A
CLNSRC
CLNACC RCV000211536.1,