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rs786204132

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786204132(A;G)
Make rs786204132(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position32127014
GeneSPAST
is asnp
is mentioned by
dbSNPrs786204132
ebirs786204132
HLIrs786204132
Exacrs786204132
Varsomers786204132
Maprs786204132
PheGenIrs786204132
hapmaprs786204132
1000 genomesrs786204132
hgdprs786204132
ensemblrs786204132
gopubmedrs786204132
geneviewrs786204132
scholarrs786204132
googlers786204132
pharmgkbrs786204132
gwascentralrs786204132
openSNPrs786204132
23andMers786204132
23andMe allrs786204132
SNP Nexus

SNPshotrs786204132
SNPdbers786204132
MSV3drs786204132
GWAS Ctlgrs786204132
Max Magnitude0
ClinVar
Risk rs786204132(G;G)
Alt rs786204132(G;G)
Reference rs786204132(A;A)
Significance Pathogenic
Disease Spastic paraplegia 4
Variation info
Gene SPAST
CLNDBN Spastic paraplegia 4, autosomal dominant
Reversed 0
HGVS NC_000002.11:g.32352083A>G
CLNSRC
CLNACC RCV000168104.1,