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rs121918089

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121918089(A;G)
Make rs121918089(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position31598610
GeneTTR
is asnp
is mentioned by
dbSNPrs121918089
ebirs121918089
HLIrs121918089
Exacrs121918089
Varsomers121918089
Maprs121918089
PheGenIrs121918089
hapmaprs121918089
1000 genomesrs121918089
hgdprs121918089
ensemblrs121918089
gopubmedrs121918089
geneviewrs121918089
scholarrs121918089
googlers121918089
pharmgkbrs121918089
gwascentralrs121918089
openSNPrs121918089
23andMers121918089
23andMe allrs121918089
SNP Nexus

SNPshotrs121918089
SNPdbers121918089
MSV3drs121918089
GWAS Ctlgrs121918089
Max Magnitude0
OMIM176300
Desc
Variant0034
Relatedalso
ClinVar
Risk rs121918089(G;G)
Alt rs121918089(G;G)
Reference rs121918089(A;A)
Significance Pathogenic
Disease Amyloidogenic transthyretin amyloidosis
Variation info
Gene TTR
CLNDBN Amyloidogenic transthyretin amyloidosis
Reversed 0
HGVS NC_000018.9:g.29178573A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000014392.17,