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rs1057518873

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518873(C;G)
Make rs1057518873(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position32144990
GeneSPAST
is asnp
is mentioned by
dbSNPrs1057518873
dbSNP (old)rs1057518873
ClinGenrs1057518873
ebirs1057518873
HLIrs1057518873
Exacrs1057518873
Gnomadrs1057518873
Varsomers1057518873
LitVarrs1057518873
Maprs1057518873
PheGenIrs1057518873
Biobankrs1057518873
1000 genomesrs1057518873
hgdprs1057518873
ensemblrs1057518873
gopubmedrs1057518873
geneviewrs1057518873
scholarrs1057518873
googlers1057518873
pharmgkbrs1057518873
gwascentralrs1057518873
openSNPrs1057518873
23andMers1057518873
23andMe allrs1057518873
SNPshotrs1057518873
SNPdbers1057518873
MSV3drs1057518873
GWAS Ctlgrs1057518873
Max Magnitude0
ClinVar
Risk rs1057518873(G;G)
Alt rs1057518873(G;G)
Reference Rs1057518873(C;C)
Significance Probable-Pathogenic
Disease Spastic paraparesis
Variation info
Gene SPAST
CLNDBN Spastic paraparesis
Reversed 0
HGVS NC_000002.11:g.32370059C>G
CLNSRC
CLNACC RCV000415025.1,