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rs1060502227

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060502227(C;G)
Make rs1060502227(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position32136593
GeneSPAST
is asnp
is mentioned by
dbSNPrs1060502227
dbSNP (old)rs1060502227
ClinGenrs1060502227
ebirs1060502227
HLIrs1060502227
Exacrs1060502227
Gnomadrs1060502227
Varsomers1060502227
LitVarrs1060502227
Maprs1060502227
PheGenIrs1060502227
Biobankrs1060502227
1000 genomesrs1060502227
hgdprs1060502227
ensemblrs1060502227
gopubmedrs1060502227
geneviewrs1060502227
scholarrs1060502227
googlers1060502227
pharmgkbrs1060502227
gwascentralrs1060502227
openSNPrs1060502227
23andMers1060502227
23andMe allrs1060502227
SNPshotrs1060502227
SNPdbers1060502227
MSV3drs1060502227
GWAS Ctlgrs1060502227
Max Magnitude0
ClinVar
Risk rs1060502227(G;G)
Alt rs1060502227(G;G)
Reference Rs1060502227(C;C)
Significance Pathogenic
Disease Spastic paraplegia 4 not provided
Variation info
Gene SPAST
CLNDBN Spastic paraplegia 4, autosomal dominant not provided
Reversed 0
HGVS NC_000002.11:g.32361662C>G
CLNSRC
CLNACC RCV000459046.1, RCV000482415.1,