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rs1060499768

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060499768(-;-)
Make rs1060499768(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position44584505
GeneSPG11
is asnp
is mentioned by
dbSNPrs1060499768
dbSNP (old)rs1060499768
ClinGenrs1060499768
ebirs1060499768
HLIrs1060499768
Exacrs1060499768
Gnomadrs1060499768
Varsomers1060499768
LitVarrs1060499768
Maprs1060499768
PheGenIrs1060499768
Biobankrs1060499768
1000 genomesrs1060499768
hgdprs1060499768
ensemblrs1060499768
gopubmedrs1060499768
geneviewrs1060499768
scholarrs1060499768
googlers1060499768
pharmgkbrs1060499768
gwascentralrs1060499768
openSNPrs1060499768
23andMers1060499768
23andMe allrs1060499768
SNPshotrs1060499768
SNPdbers1060499768
MSV3drs1060499768
GWAS Ctlgrs1060499768
Max Magnitude0
ClinVar
Risk rs1060499768(-;-)
Alt rs1060499768(-;-)
Reference Rs1060499768(A;A)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene SPG11
CLNDBN Abnormality of brain morphology
Reversed 1
HGVS NC_000015.9:g.44876703delT
CLNSRC
CLNACC RCV000454217.1,