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rs397516482

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516482(A;T)
Make rs397516482(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201361286
GeneTNNT2
is asnp
is mentioned by
dbSNPrs397516482
ebirs397516482
HLIrs397516482
Exacrs397516482
Varsomers397516482
Maprs397516482
PheGenIrs397516482
hapmaprs397516482
1000 genomesrs397516482
hgdprs397516482
ensemblrs397516482
gopubmedrs397516482
geneviewrs397516482
scholarrs397516482
googlers397516482
pharmgkbrs397516482
gwascentralrs397516482
openSNPrs397516482
23andMers397516482
23andMe allrs397516482
SNP Nexus

SNPshotrs397516482
SNPdbers397516482
MSV3drs397516482
GWAS Ctlgrs397516482
Max Magnitude0
ClinVar
Risk rs397516482(T;T)
Alt rs397516482(T;T)
Reference rs397516482(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene TNNT2
CLNDBN not specified
Reversed 1
HGVS NC_000001.10:g.201330414T>A
CLNSRC
CLNACC RCV000036618.2,