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rs397516345

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516345(C;T)
Make rs397516345(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55154745
GeneTNNI3
is asnp
is mentioned by
dbSNPrs397516345
dbSNP (classic)rs397516345
ClinGenrs397516345
ebirs397516345
HLIrs397516345
Exacrs397516345
Gnomadrs397516345
Varsomers397516345
LitVarrs397516345
Maprs397516345
PheGenIrs397516345
Biobankrs397516345
1000 genomesrs397516345
hgdprs397516345
ensemblrs397516345
geneviewrs397516345
scholarrs397516345
googlers397516345
pharmgkbrs397516345
gwascentralrs397516345
openSNPrs397516345
23andMers397516345
SNPshotrs397516345
SNPdbers397516345
MSV3drs397516345
GWAS Ctlgrs397516345
Max Magnitude0
ClinVar
Risk rs397516345(T;T)
Alt rs397516345(T;T)
Reference Rs397516345(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene TNNI3
CLNDBN not specified
Reversed 1
HGVS NC_000019.9:g.55666113G>A
CLNSRC
CLNACC RCV000036285.2,