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rs121918099

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121918099(C;C)
Make rs121918099(C;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position31595170
GeneTTR
is asnp
is mentioned by
dbSNPrs121918099
ebirs121918099
HLIrs121918099
Exacrs121918099
Varsomers121918099
Maprs121918099
PheGenIrs121918099
hapmaprs121918099
1000 genomesrs121918099
hgdprs121918099
ensemblrs121918099
gopubmedrs121918099
geneviewrs121918099
scholarrs121918099
googlers121918099
pharmgkbrs121918099
gwascentralrs121918099
openSNPrs121918099
23andMers121918099
23andMe allrs121918099
SNP Nexus

SNPshotrs121918099
SNPdbers121918099
MSV3drs121918099
GWAS Ctlgrs121918099
Merged fromRs28933983
Max Magnitude0
OMIM176300
Desc
Variant0048
Relatedalso
ClinVar
Risk rs121918099(C;C)
Alt rs121918099(C;C)
Reference rs121918099(T;T)
Significance Untested
Disease
Variation info
Gene TTR
CLNDBN
Reversed 0
HGVS NC_000018.9:g.29175133T>C
CLNSRC
CLNACC