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rs121918074

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918074(A;A)
Make rs121918074(A;C)
ReferenceGRCh38 38.1/141
Chromosome18
Position31595247
GeneTTR
is asnp
is mentioned by
dbSNPrs121918074
ebirs121918074
HLIrs121918074
Exacrs121918074
Varsomers121918074
Maprs121918074
PheGenIrs121918074
hapmaprs121918074
1000 genomesrs121918074
hgdprs121918074
ensemblrs121918074
gopubmedrs121918074
geneviewrs121918074
scholarrs121918074
googlers121918074
pharmgkbrs121918074
gwascentralrs121918074
openSNPrs121918074
23andMers121918074
23andMe allrs121918074
SNP Nexus

SNPshotrs121918074
SNPdbers121918074
MSV3drs121918074
GWAS Ctlgrs121918074
Max Magnitude0
OMIM176300
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121918074(A;A)
Alt rs121918074(A;A)
Reference rs121918074(C;C)
Significance Other
Disease Amyloidogenic transthyretin amyloidosis not specified
Variation info
Gene TTR
CLNDBN Amyloidogenic transthyretin amyloidosis not specified
Reversed 0
HGVS NC_000018.9:g.29175210C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014369.27, RCV000152541.1,