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rs387906523

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906523(C;C)
Make rs387906523(C;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position31593025
GeneTTR
is asnp
is mentioned by
dbSNPrs387906523
ebirs387906523
HLIrs387906523
Exacrs387906523
Varsomers387906523
Maprs387906523
PheGenIrs387906523
hapmaprs387906523
1000 genomesrs387906523
hgdprs387906523
ensemblrs387906523
gopubmedrs387906523
geneviewrs387906523
scholarrs387906523
googlers387906523
pharmgkbrs387906523
gwascentralrs387906523
openSNPrs387906523
23andMers387906523
23andMe allrs387906523
SNP Nexus

SNPshotrs387906523
SNPdbers387906523
MSV3drs387906523
GWAS Ctlgrs387906523
Max Magnitude0
ClinVar
Risk rs387906523(A,C;A,C)
Alt rs387906523(A,C;A,C)
Reference rs387906523(G;G)
Significance Pathogenic
Disease Amyloidogenic transthyretin amyloidosis
Variation info
Gene TTR
CLNDBN Amyloidogenic transthyretin amyloidosis
Reversed 0
HGVS NC_000018.9:g.29172988G>A; NC_000018.9:g.29172988G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000014401.26, RCV000014378.25,