Have questions? Visit https://www.reddit.com/r/SNPedia

rs397516359

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516359(C;T)
Make rs397516359(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position55157585
GeneTNNI3
is asnp
is mentioned by
dbSNPrs397516359
ebirs397516359
HLIrs397516359
Exacrs397516359
Varsomers397516359
Maprs397516359
PheGenIrs397516359
hapmaprs397516359
1000 genomesrs397516359
hgdprs397516359
ensemblrs397516359
gopubmedrs397516359
geneviewrs397516359
scholarrs397516359
googlers397516359
pharmgkbrs397516359
gwascentralrs397516359
openSNPrs397516359
23andMers397516359
23andMe allrs397516359
SNP Nexus

SNPshotrs397516359
SNPdbers397516359
MSV3drs397516359
GWAS Ctlgrs397516359
Max Magnitude0
ClinVar
Risk rs397516359(T;T)
Alt rs397516359(T;T)
Reference rs397516359(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene TNNI3
CLNDBN not specified
Reversed 1
HGVS NC_000019.9:g.55668953G>A
CLNSRC ClinVar
CLNACC RCV000036309.3,