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rs121909214

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121909214(C;C)
Make rs121909214(C;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position136056736
GeneTGFBI
is asnp
is mentioned by
dbSNPrs121909214
ebirs121909214
HLIrs121909214
Exacrs121909214
Varsomers121909214
Maprs121909214
PheGenIrs121909214
hapmaprs121909214
1000 genomesrs121909214
hgdprs121909214
ensemblrs121909214
gopubmedrs121909214
geneviewrs121909214
scholarrs121909214
googlers121909214
pharmgkbrs121909214
gwascentralrs121909214
openSNPrs121909214
23andMers121909214
23andMe allrs121909214
SNP Nexus

SNPshotrs121909214
SNPdbers121909214
MSV3drs121909214
GWAS Ctlgrs121909214
Max Magnitude0
OMIM601692
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121909214(C;C)
Alt rs121909214(C;C)
Reference rs121909214(T;T)
Significance Pathogenic
Disease Lattice corneal dystrophy type 3A
Variation info
Gene TGFBI
CLNDBN Lattice corneal dystrophy type 3A
Reversed 0
HGVS NC_000005.9:g.135392425T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000008324.2,