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rs1085307118

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome22
Position18169868
GeneUSP18
is asnp
is mentioned by
dbSNPrs1085307118
dbSNP (old)rs1085307118
ClinGenrs1085307118
ebirs1085307118
HLIrs1085307118
Exacrs1085307118
Gnomadrs1085307118
Varsomers1085307118
Maprs1085307118
PheGenIrs1085307118
Biobankrs1085307118
1000 genomesrs1085307118
hgdprs1085307118
ensemblrs1085307118
gopubmedrs1085307118
geneviewrs1085307118
scholarrs1085307118
googlers1085307118
pharmgkbrs1085307118
gwascentralrs1085307118
openSNPrs1085307118
23andMers1085307118
23andMe allrs1085307118
SNPshotrs1085307118
SNPdbers1085307118
MSV3drs1085307118
GWAS Ctlgrs1085307118
Max Magnitude0
ClinVar
Risk rs1085307118(T;T)
Alt rs1085307118(T;T)
Reference Rs1085307118(C;C)
Significance Pathogenic
Disease Pseudo-torch syndrome 2
Variation info
Gene USP18
CLNDBN Pseudo-torch syndrome 2
Reversed 0
HGVS NC_000022.10:g.18652635C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000477724.1,