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rs397516466

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516466(A;A)
Make rs397516466(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position201364341
GeneTNNT2
is asnp
is mentioned by
dbSNPrs397516466
ebirs397516466
HLIrs397516466
Exacrs397516466
Varsomers397516466
Maprs397516466
PheGenIrs397516466
hapmaprs397516466
1000 genomesrs397516466
hgdprs397516466
ensemblrs397516466
gopubmedrs397516466
geneviewrs397516466
scholarrs397516466
googlers397516466
pharmgkbrs397516466
gwascentralrs397516466
openSNPrs397516466
23andMers397516466
23andMe allrs397516466
SNP Nexus

SNPshotrs397516466
SNPdbers397516466
MSV3drs397516466
GWAS Ctlgrs397516466
Max Magnitude0
ClinVar
Risk rs397516466(A;A)
Alt rs397516466(A;A)
Reference rs397516466(G;G)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene TNNT2
CLNDBN not specified not provided
Reversed 1
HGVS NC_000001.10:g.201333469C>T
CLNSRC ClinVar
CLNACC RCV000036590.3, RCV000159295.2,