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rs397516452

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516452(C;C)
Make rs397516452(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position201365623
GeneTNNT2
is asnp
is mentioned by
dbSNPrs397516452
ebirs397516452
HLIrs397516452
Exacrs397516452
Varsomers397516452
Maprs397516452
PheGenIrs397516452
hapmaprs397516452
1000 genomesrs397516452
hgdprs397516452
ensemblrs397516452
gopubmedrs397516452
geneviewrs397516452
scholarrs397516452
googlers397516452
pharmgkbrs397516452
gwascentralrs397516452
openSNPrs397516452
23andMers397516452
23andMe allrs397516452
SNP Nexus

SNPshotrs397516452
SNPdbers397516452
MSV3drs397516452
GWAS Ctlgrs397516452
Max Magnitude0
ClinVar
Risk rs397516452(C;C)
Alt rs397516452(C;C)
Reference rs397516452(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.201334751C>G
CLNSRC
CLNACC RCV000036568.3, RCV000159277.2,