Have questions? Visit https://www.reddit.com/r/SNPedia

rs121918073

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918073(A;A)
Make rs121918073(A;C)
ReferenceGRCh38 38.1/141
Chromosome18
Position31598622
GeneTTR
is asnp
is mentioned by
dbSNPrs121918073
ebirs121918073
HLIrs121918073
Exacrs121918073
Varsomers121918073
Maprs121918073
PheGenIrs121918073
hapmaprs121918073
1000 genomesrs121918073
hgdprs121918073
ensemblrs121918073
gopubmedrs121918073
geneviewrs121918073
scholarrs121918073
googlers121918073
pharmgkbrs121918073
gwascentralrs121918073
openSNPrs121918073
23andMers121918073
23andMe allrs121918073
SNP Nexus

SNPshotrs121918073
SNPdbers121918073
MSV3drs121918073
GWAS Ctlgrs121918073
Max Magnitude0
OMIM176300
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121918073(A;A)
Alt rs121918073(A;A)
Reference rs121918073(C;C)
Significance Pathogenic
Disease Amyloidogenic transthyretin amyloidosis
Variation info
Gene TTR
CLNDBN Amyloidogenic transthyretin amyloidosis
Reversed 0
HGVS NC_000018.9:g.29178585C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014366.26,