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rs786204163

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204163(C;C)
Make rs786204163(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position32137108
GeneSPAST
is asnp
is mentioned by
dbSNPrs786204163
ebirs786204163
HLIrs786204163
Exacrs786204163
Varsomers786204163
Maprs786204163
PheGenIrs786204163
hapmaprs786204163
1000 genomesrs786204163
hgdprs786204163
ensemblrs786204163
gopubmedrs786204163
geneviewrs786204163
scholarrs786204163
googlers786204163
pharmgkbrs786204163
gwascentralrs786204163
openSNPrs786204163
23andMers786204163
23andMe allrs786204163
SNP Nexus

SNPshotrs786204163
SNPdbers786204163
MSV3drs786204163
GWAS Ctlgrs786204163
Max Magnitude0
ClinVar
Risk rs786204163(C;C)
Alt rs786204163(C;C)
Reference rs786204163(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.32362177G>C
CLNSRC
CLNACC RCV000168164.1,