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rs121918092

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918092(C;T)
Make rs121918092(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position31598617
GeneTTR
is asnp
is mentioned by
dbSNPrs121918092
ebirs121918092
HLIrs121918092
Exacrs121918092
Varsomers121918092
Maprs121918092
PheGenIrs121918092
hapmaprs121918092
1000 genomesrs121918092
hgdprs121918092
ensemblrs121918092
gopubmedrs121918092
geneviewrs121918092
scholarrs121918092
googlers121918092
pharmgkbrs121918092
gwascentralrs121918092
openSNPrs121918092
23andMers121918092
23andMe allrs121918092
SNP Nexus

SNPshotrs121918092
SNPdbers121918092
MSV3drs121918092
GWAS Ctlgrs121918092
Merged fromRs28933982
Max Magnitude0
OMIM176300
Desc
Variant0038
Relatedalso
ClinVar
Risk rs121918092(T;T)
Alt rs121918092(T;T)
Reference rs121918092(C;C)
Significance Other
Disease Dystransthyretinemic euthyroidal hyperthyroxinemia
Variation info
Gene TTR
CLNDBN Dystransthyretinemic euthyroidal hyperthyroxinemia
Reversed 0
HGVS NC_000018.9:g.29178580C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014396.26,