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rs397516348

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516348(A;A)
Make rs397516348(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55154151
GeneTNNI3
is asnp
is mentioned by
dbSNPrs397516348
ebirs397516348
HLIrs397516348
Exacrs397516348
Varsomers397516348
Maprs397516348
PheGenIrs397516348
hapmaprs397516348
1000 genomesrs397516348
hgdprs397516348
ensemblrs397516348
gopubmedrs397516348
geneviewrs397516348
scholarrs397516348
googlers397516348
pharmgkbrs397516348
gwascentralrs397516348
openSNPrs397516348
23andMers397516348
23andMe allrs397516348
SNP Nexus

SNPshotrs397516348
SNPdbers397516348
MSV3drs397516348
GWAS Ctlgrs397516348
Max Magnitude0
ClinVar
Risk rs397516348(A;A)
Alt rs397516348(A;A)
Reference rs397516348(C;C)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene TNNI3
CLNDBN not specified not provided
Reversed 1
HGVS NC_000019.9:g.55665519G>T
CLNSRC
CLNACC RCV000036291.2, RCV000159221.2,