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rs397516465

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516465(C;T)
Make rs397516465(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201364342
GeneTNNT2
is asnp
is mentioned by
dbSNPrs397516465
ebirs397516465
HLIrs397516465
Exacrs397516465
Varsomers397516465
Maprs397516465
PheGenIrs397516465
hapmaprs397516465
1000 genomesrs397516465
hgdprs397516465
ensemblrs397516465
gopubmedrs397516465
geneviewrs397516465
scholarrs397516465
googlers397516465
pharmgkbrs397516465
gwascentralrs397516465
openSNPrs397516465
23andMers397516465
23andMe allrs397516465
SNP Nexus

SNPshotrs397516465
SNPdbers397516465
MSV3drs397516465
GWAS Ctlgrs397516465
Max Magnitude0
ClinVar
Risk rs397516465(T;T)
Alt rs397516465(T;T)
Reference rs397516465(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene TNNT2
CLNDBN not specified
Reversed 1
HGVS NC_000001.10:g.201333470G>A
CLNSRC
CLNACC RCV000036588.3,