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rs1060499753

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060499753(-;-)
Make rs1060499753(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position83683022
GeneUBQLN1
is asnp
is mentioned by
dbSNPrs1060499753
dbSNP (old)rs1060499753
ClinGenrs1060499753
ebirs1060499753
HLIrs1060499753
Exacrs1060499753
Gnomadrs1060499753
Varsomers1060499753
LitVarrs1060499753
Maprs1060499753
PheGenIrs1060499753
Biobankrs1060499753
1000 genomesrs1060499753
hgdprs1060499753
ensemblrs1060499753
gopubmedrs1060499753
geneviewrs1060499753
scholarrs1060499753
googlers1060499753
pharmgkbrs1060499753
gwascentralrs1060499753
openSNPrs1060499753
23andMers1060499753
23andMe allrs1060499753
SNPshotrs1060499753
SNPdbers1060499753
MSV3drs1060499753
GWAS Ctlgrs1060499753
Max Magnitude0
ClinVar
Risk rs1060499753(-;-)
Alt rs1060499753(-;-)
Reference Rs1060499753(A;A)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene UBQLN1
CLNDBN Abnormality of brain morphology
Reversed 1
HGVS NC_000009.11:g.86297937delT
CLNSRC
CLNACC RCV000454188.1,