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rs397516343

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516343(G;T)
Make rs397516343(T;T)
ReferenceGRCh38 38.1/142
Chromosome19
Position55156237
GeneTNNI3
is asnp
is mentioned by
dbSNPrs397516343
ebirs397516343
HLIrs397516343
Exacrs397516343
Varsomers397516343
Maprs397516343
PheGenIrs397516343
hapmaprs397516343
1000 genomesrs397516343
hgdprs397516343
ensemblrs397516343
gopubmedrs397516343
geneviewrs397516343
scholarrs397516343
googlers397516343
pharmgkbrs397516343
gwascentralrs397516343
openSNPrs397516343
23andMers397516343
23andMe allrs397516343
SNP Nexus

SNPshotrs397516343
SNPdbers397516343
MSV3drs397516343
GWAS Ctlgrs397516343
Max Magnitude0
ClinVar
Risk rs397516343(A,T;A,T)
Alt rs397516343(A,T;A,T)
Reference rs397516343(G;G)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene TNNI3
CLNDBN not specified
Reversed 1
HGVS NC_000019.9:g.55667605C>A
CLNSRC ClinVar
CLNACC RCV000036278.2,