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rs1060502226

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060502226(A;A)
Make rs1060502226(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position32127023
GeneSPAST
is asnp
is mentioned by
dbSNPrs1060502226
dbSNP (old)rs1060502226
ClinGenrs1060502226
ebirs1060502226
HLIrs1060502226
Exacrs1060502226
Gnomadrs1060502226
Varsomers1060502226
Maprs1060502226
PheGenIrs1060502226
Biobankrs1060502226
1000 genomesrs1060502226
hgdprs1060502226
ensemblrs1060502226
gopubmedrs1060502226
geneviewrs1060502226
scholarrs1060502226
googlers1060502226
pharmgkbrs1060502226
gwascentralrs1060502226
openSNPrs1060502226
23andMers1060502226
23andMe allrs1060502226
SNPshotrs1060502226
SNPdbers1060502226
MSV3drs1060502226
GWAS Ctlgrs1060502226
Max Magnitude0
ClinVar
Risk rs1060502226(A;A)
Alt rs1060502226(A;A)
Reference Rs1060502226(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.32352092G>A
CLNSRC
CLNACC RCV000472388.1,