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rs11541790

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs11541790(A;A)
Make rs11541790(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome18
Position31592956
GeneTTR
is asnp
is mentioned by
dbSNPrs11541790
ebirs11541790
HLIrs11541790
Exacrs11541790
Varsomers11541790
Maprs11541790
PheGenIrs11541790
hapmaprs11541790
1000 genomesrs11541790
hgdprs11541790
ensemblrs11541790
gopubmedrs11541790
geneviewrs11541790
scholarrs11541790
googlers11541790
pharmgkbrs11541790
gwascentralrs11541790
openSNPrs11541790
23andMers11541790
23andMe allrs11541790
SNP Nexus

SNPshotrs11541790
SNPdbers11541790
MSV3drs11541790
GWAS Ctlgrs11541790
Max Magnitude0
? (A;A) (A;G) (G;G) 28
ClinVar
Risk rs11541790(A;A)
Alt rs11541790(A;A)
Reference rs11541790(G;G)
Significance Other
Disease not provided
Variation info
Gene TTR
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.29172919C>T
CLNSRC
CLNACC RCV000159421.2,