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rs1060499670

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499670(C;T)
Make rs1060499670(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position32126960
GeneSPAST
is asnp
is mentioned by
dbSNPrs1060499670
dbSNP (classic)rs1060499670
ClinGenrs1060499670
ebirs1060499670
HLIrs1060499670
Exacrs1060499670
Gnomadrs1060499670
Varsomers1060499670
LitVarrs1060499670
Maprs1060499670
PheGenIrs1060499670
Biobankrs1060499670
1000 genomesrs1060499670
hgdprs1060499670
ensemblrs1060499670
geneviewrs1060499670
scholarrs1060499670
googlers1060499670
pharmgkbrs1060499670
gwascentralrs1060499670
openSNPrs1060499670
23andMers1060499670
23andMe allrs1060499670
SNPshotrs1060499670
SNPdbers1060499670
MSV3drs1060499670
GWAS Ctlgrs1060499670
Max Magnitude0
ClinVar
Risk rs1060499670(T;T)
Alt rs1060499670(T;T)
Reference Rs1060499670(C;C)
Significance Probable-Pathogenic
Disease Spastic paraplegia 4
Variation info
Gene SPAST
CLNDBN Spastic paraplegia 4, autosomal dominant
Reversed 0
HGVS NC_000002.11:g.32352029C>T
CLNSRC
CLNACC RCV000449607.1,