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rs121918087

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918087(C;G)
Make rs121918087(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position31598581
GeneTTR
is asnp
is mentioned by
dbSNPrs121918087
ebirs121918087
HLIrs121918087
Exacrs121918087
Varsomers121918087
Maprs121918087
PheGenIrs121918087
hapmaprs121918087
1000 genomesrs121918087
hgdprs121918087
ensemblrs121918087
gopubmedrs121918087
geneviewrs121918087
scholarrs121918087
googlers121918087
pharmgkbrs121918087
gwascentralrs121918087
openSNPrs121918087
23andMers121918087
23andMe allrs121918087
SNP Nexus

SNPshotrs121918087
SNPdbers121918087
MSV3drs121918087
GWAS Ctlgrs121918087
Max Magnitude0
OMIM176300
Desc
Variant0032
Relatedalso
ClinVar
Risk rs121918087(G;G)
Alt rs121918087(G;G)
Reference rs121918087(C;C)
Significance Pathogenic
Disease Amyloidogenic transthyretin amyloidosis
Variation info
Gene TTR
CLNDBN Amyloidogenic transthyretin amyloidosis
Reversed 0
HGVS NC_000018.9:g.29178544C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000014390.24,