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rs1085307141

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome10
Position17230709
GeneVIM, VIM-AS1
is asnp
is mentioned by
dbSNPrs1085307141
dbSNP (old)rs1085307141
ClinGenrs1085307141
ebirs1085307141
HLIrs1085307141
Exacrs1085307141
Gnomadrs1085307141
Varsomers1085307141
Maprs1085307141
PheGenIrs1085307141
Biobankrs1085307141
1000 genomesrs1085307141
hgdprs1085307141
ensemblrs1085307141
gopubmedrs1085307141
geneviewrs1085307141
scholarrs1085307141
googlers1085307141
pharmgkbrs1085307141
gwascentralrs1085307141
openSNPrs1085307141
23andMers1085307141
23andMe allrs1085307141
SNPshotrs1085307141
SNPdbers1085307141
MSV3drs1085307141
GWAS Ctlgrs1085307141
Max Magnitude0
ClinVar
Risk rs1085307141(G;G)
Alt rs1085307141(G;G)
Reference Rs1085307141(A;A)
Significance Pathogenic
Disease Cataract 30
Variation info
Gene VIM-AS1 VIM
CLNDBN Cataract 30, multiple types
Reversed 0
HGVS NC_000010.10:g.17272708A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000488719.1,