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

rs121918078

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918078(A;A)
Make rs121918078(A;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position31593019
GeneTTR
is asnp
is mentioned by
dbSNPrs121918078
ebirs121918078
HLIrs121918078
Exacrs121918078
Varsomers121918078
Maprs121918078
PheGenIrs121918078
hapmaprs121918078
1000 genomesrs121918078
hgdprs121918078
ensemblrs121918078
gopubmedrs121918078
geneviewrs121918078
scholarrs121918078
googlers121918078
pharmgkbrs121918078
gwascentralrs121918078
openSNPrs121918078
23andMers121918078
23andMe allrs121918078
SNP Nexus

SNPshotrs121918078
SNPdbers121918078
MSV3drs121918078
GWAS Ctlgrs121918078
Max Magnitude0
OMIM176300
Desc
Variant0021
Relatedalso
ClinVar
Risk rs121918078(A;A)
Alt rs121918078(A;A)
Reference rs121918078(G;G)
Significance Untested
Disease Amyloidogenic transthyretin amyloidosis
Variation info
Gene TTR
CLNDBN Amyloidogenic transthyretin amyloidosis
Reversed 0
HGVS NC_000018.9:g.29172982G>A
CLNSRC OMIM Allelic Variant
CLNACC SCV000034628.1, SCV000034628.1,