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rs1057518880

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518880(-;-)
Make rs1057518880(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position32126966
GeneSPAST
is asnp
is mentioned by
dbSNPrs1057518880
dbSNP (old)rs1057518880
ClinGenrs1057518880
ebirs1057518880
HLIrs1057518880
Exacrs1057518880
Gnomadrs1057518880
Varsomers1057518880
LitVarrs1057518880
Maprs1057518880
PheGenIrs1057518880
Biobankrs1057518880
1000 genomesrs1057518880
hgdprs1057518880
ensemblrs1057518880
gopubmedrs1057518880
geneviewrs1057518880
scholarrs1057518880
googlers1057518880
pharmgkbrs1057518880
gwascentralrs1057518880
openSNPrs1057518880
23andMers1057518880
23andMe allrs1057518880
SNPshotrs1057518880
SNPdbers1057518880
MSV3drs1057518880
GWAS Ctlgrs1057518880
Max Magnitude0
ClinVar
Risk rs1057518880(-;-)
Alt rs1057518880(-;-)
Reference Rs1057518880(G;G)
Significance Pathogenic
Disease Spastic paraplegia
Variation info
Gene SPAST
CLNDBN Spastic paraplegia
Reversed 0
HGVS NC_000002.11:g.32352035delG
CLNSRC
CLNACC RCV000414756.1,