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rs121918080

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918080(G;T)
Make rs121918080(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position31595128
GeneTTR
is asnp
is mentioned by
dbSNPrs121918080
ebirs121918080
HLIrs121918080
Exacrs121918080
Varsomers121918080
Maprs121918080
PheGenIrs121918080
hapmaprs121918080
1000 genomesrs121918080
hgdprs121918080
ensemblrs121918080
gopubmedrs121918080
geneviewrs121918080
scholarrs121918080
googlers121918080
pharmgkbrs121918080
gwascentralrs121918080
openSNPrs121918080
23andMers121918080
23andMe allrs121918080
SNP Nexus

SNPshotrs121918080
SNPdbers121918080
MSV3drs121918080
GWAS Ctlgrs121918080
Max Magnitude0
OMIM176300
Desc
Variant0023
Relatedalso
ClinVar
Risk rs121918080(A,T;A,T)
Alt rs121918080(A,T;A,T)
Reference rs121918080(G;G)
Significance Pathogenic
Disease Amyloidogenic transthyretin amyloidosis
Variation info
Gene TTR
CLNDBN Amyloidogenic transthyretin amyloidosis
Reversed 0
HGVS NC_000018.9:g.29175091G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014381.24,