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rs121917867

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121917867(C;G)
Make rs121917867(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position56453703
GeneMIP
is asnp
is mentioned by
dbSNPrs121917867
ebirs121917867
HLIrs121917867
Exacrs121917867
Varsomers121917867
Maprs121917867
PheGenIrs121917867
hapmaprs121917867
1000 genomesrs121917867
hgdprs121917867
ensemblrs121917867
gopubmedrs121917867
geneviewrs121917867
scholarrs121917867
googlers121917867
pharmgkbrs121917867
gwascentralrs121917867
openSNPrs121917867
23andMers121917867
23andMe allrs121917867
SNP Nexus

SNPshotrs121917867
SNPdbers121917867
MSV3drs121917867
GWAS Ctlgrs121917867
Max Magnitude0
ClinVar
Risk rs121917867(G,T;G,T)
Alt rs121917867(G,T;G,T)
Reference rs121917867(C;C)
Significance Pathogenic
Disease Cataract 15
Variation info
Gene MIP
CLNDBN Cataract 15, multiple types
Reversed 1
HGVS NC_000012.11:g.56847487G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000015428.26,