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rs730881169

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881169(A;A)
Make rs730881169(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome18
Position31593020
GeneTTR
is asnp
is mentioned by
dbSNPrs730881169
ebirs730881169
HLIrs730881169
Exacrs730881169
Varsomers730881169
Maprs730881169
PheGenIrs730881169
hapmaprs730881169
1000 genomesrs730881169
hgdprs730881169
ensemblrs730881169
gopubmedrs730881169
geneviewrs730881169
scholarrs730881169
googlers730881169
pharmgkbrs730881169
gwascentralrs730881169
openSNPrs730881169
23andMers730881169
23andMe allrs730881169
SNP Nexus

SNPshotrs730881169
SNPdbers730881169
MSV3drs730881169
GWAS Ctlgrs730881169
Max Magnitude0
ClinVar
Risk rs730881169(A;A)
Alt rs730881169(A;A)
Reference rs730881169(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTR
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.29172983C>A
CLNSRC
CLNACC RCV000159436.1,