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rs730881166

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881166(C;T)
Make rs730881166(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome18
Position31598628
GeneTTR
is asnp
is mentioned by
dbSNPrs730881166
ebirs730881166
HLIrs730881166
Exacrs730881166
Varsomers730881166
Maprs730881166
PheGenIrs730881166
hapmaprs730881166
1000 genomesrs730881166
hgdprs730881166
ensemblrs730881166
gopubmedrs730881166
geneviewrs730881166
scholarrs730881166
googlers730881166
pharmgkbrs730881166
gwascentralrs730881166
openSNPrs730881166
23andMers730881166
23andMe allrs730881166
SNP Nexus

SNPshotrs730881166
SNPdbers730881166
MSV3drs730881166
GWAS Ctlgrs730881166
Max Magnitude0
ClinVar
Risk rs730881166(T;T)
Alt rs730881166(T;T)
Reference rs730881166(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTR
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.29178591C>T
CLNSRC
CLNACC RCV000159432.2,