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rs121918096

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GTC;GTC) 0 common in clinvar
Make rs121918096(-;-)
Make rs121918096(-;GTC)
ReferenceGRCh38 38.1/141
Chromosome18
Position31598655
GeneTTR
is asnp
is mentioned by
dbSNPrs121918096
ebirs121918096
HLIrs121918096
Exacrs121918096
Varsomers121918096
Maprs121918096
PheGenIrs121918096
hapmaprs121918096
1000 genomesrs121918096
hgdprs121918096
ensemblrs121918096
gopubmedrs121918096
geneviewrs121918096
scholarrs121918096
googlers121918096
pharmgkbrs121918096
gwascentralrs121918096
openSNPrs121918096
23andMers121918096
23andMe allrs121918096
SNP Nexus

SNPshotrs121918096
SNPdbers121918096
MSV3drs121918096
GWAS Ctlgrs121918096
Max Magnitude0
OMIM176300
Desc
Variant0044
Relatedalso
ClinVar
Risk rs121918096(;)
Alt rs121918096(;)
Reference rs121918096(GTC;GTC)
Significance Other
Disease Amyloidogenic transthyretin amyloidosis
Variation info
Gene TTR
CLNDBN Amyloidogenic transthyretin amyloidosis
Reversed 0
HGVS NC_000018.9:g.29178618_29178620delGTC
CLNSRC OMIM Allelic Variant
CLNACC RCV000014402.28,