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rs730881167

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881167(A;C)
Make rs730881167(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome18
Position31598638
GeneTTR
is asnp
is mentioned by
dbSNPrs730881167
ebirs730881167
HLIrs730881167
Exacrs730881167
Varsomers730881167
Maprs730881167
PheGenIrs730881167
hapmaprs730881167
1000 genomesrs730881167
hgdprs730881167
ensemblrs730881167
gopubmedrs730881167
geneviewrs730881167
scholarrs730881167
googlers730881167
pharmgkbrs730881167
gwascentralrs730881167
openSNPrs730881167
23andMers730881167
23andMe allrs730881167
SNP Nexus

SNPshotrs730881167
SNPdbers730881167
MSV3drs730881167
GWAS Ctlgrs730881167
Max Magnitude0
ClinVar
Risk rs730881167(C;C)
Alt rs730881167(C;C)
Reference rs730881167(A;A)
Significance Pathogenic
Disease Cardiomyopathy not provided
Variation info
Gene TTR
CLNDBN Cardiomyopathy not provided
Reversed 0
HGVS NC_000018.9:g.29178601A>C
CLNSRC
CLNACC RCV000159433.1, RCV000223926.1,