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rs121918095

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918095(A;A)
Make rs121918095(A;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position31598602
GeneTTR
is asnp
is mentioned by
dbSNPrs121918095
ebirs121918095
HLIrs121918095
Exacrs121918095
Varsomers121918095
Maprs121918095
PheGenIrs121918095
hapmaprs121918095
1000 genomesrs121918095
hgdprs121918095
ensemblrs121918095
gopubmedrs121918095
geneviewrs121918095
scholarrs121918095
googlers121918095
pharmgkbrs121918095
gwascentralrs121918095
openSNPrs121918095
23andMers121918095
23andMe allrs121918095
SNP Nexus

SNPshotrs121918095
SNPdbers121918095
MSV3drs121918095
GWAS Ctlgrs121918095
GMAF0.003673
Max Magnitude0
OMIM176300
Desc
Variant0042
Relatedalso
ClinVar
Risk rs121918095(A;A)
Alt rs121918095(A;A)
Reference rs121918095(G;G)
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.29178565G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014400.27, RCV000152543.1,