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rs121917775

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121917775(A;A)
Make rs121917775(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position17229873
GeneVIM
is asnp
is mentioned by
dbSNPrs121917775
ebirs121917775
HLIrs121917775
Exacrs121917775
Varsomers121917775
Maprs121917775
PheGenIrs121917775
hapmaprs121917775
1000 genomesrs121917775
hgdprs121917775
ensemblrs121917775
gopubmedrs121917775
geneviewrs121917775
scholarrs121917775
googlers121917775
pharmgkbrs121917775
gwascentralrs121917775
openSNPrs121917775
23andMers121917775
23andMe allrs121917775
SNP Nexus

SNPshotrs121917775
SNPdbers121917775
MSV3drs121917775
GWAS Ctlgrs121917775
Max Magnitude0
OMIM193060
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121917775(A;A)
Alt rs121917775(A;A)
Reference rs121917775(G;G)
Significance Pathogenic
Disease Cataract 30 not provided
Variation info
Gene VIM-AS1 VIM
CLNDBN Cataract 30 not provided
Reversed 0
HGVS NC_000010.10:g.17271872G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012983.24, RCV000056967.1,