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rs1085307110

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome3
Position134650909
is asnp
is mentioned by
dbSNPrs1085307110
dbSNP (old)rs1085307110
ClinGenrs1085307110
ebirs1085307110
HLIrs1085307110
Exacrs1085307110
Gnomadrs1085307110
Varsomers1085307110
Maprs1085307110
PheGenIrs1085307110
Biobankrs1085307110
1000 genomesrs1085307110
hgdprs1085307110
ensemblrs1085307110
gopubmedrs1085307110
geneviewrs1085307110
scholarrs1085307110
googlers1085307110
pharmgkbrs1085307110
gwascentralrs1085307110
openSNPrs1085307110
23andMers1085307110
23andMe allrs1085307110
SNPshotrs1085307110
SNPdbers1085307110
MSV3drs1085307110
GWAS Ctlgrs1085307110
Max Magnitude0
ClinVar
Risk rs1085307110(.;.)
Alt rs1085307110(.;.)
Reference Rs1085307110(T;T)
Significance Pathogenic
Disease Hereditary spastic paraplegia
Variation info
Gene LOC101927568
CLNDBN Hereditary spastic paraplegia
Reversed 1
HGVS NC_000003.11:g.134369751_134369752insATGTCGATAGATACAGCACATGTCGATA
CLNSRC
CLNACC RCV000488883.1,