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rs730881163

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881163(A;A)
Make rs730881163(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome18
Position31595155
GeneTTR
is asnp
is mentioned by
dbSNPrs730881163
ebirs730881163
HLIrs730881163
Exacrs730881163
Varsomers730881163
Maprs730881163
PheGenIrs730881163
hapmaprs730881163
1000 genomesrs730881163
hgdprs730881163
ensemblrs730881163
gopubmedrs730881163
geneviewrs730881163
scholarrs730881163
googlers730881163
pharmgkbrs730881163
gwascentralrs730881163
openSNPrs730881163
23andMers730881163
23andMe allrs730881163
SNP Nexus

SNPshotrs730881163
SNPdbers730881163
MSV3drs730881163
GWAS Ctlgrs730881163
Max Magnitude0
ClinVar
Risk rs730881163(A;A)
Alt rs730881163(A;A)
Reference rs730881163(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TTR
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.29175118C>A
CLNSRC
CLNACC RCV000159426.2,