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rs397516376

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516376(C;T)
Make rs397516376(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position63060924
GeneTPM1
is asnp
is mentioned by
dbSNPrs397516376
ebirs397516376
HLIrs397516376
Exacrs397516376
Varsomers397516376
Maprs397516376
PheGenIrs397516376
hapmaprs397516376
1000 genomesrs397516376
hgdprs397516376
ensemblrs397516376
gopubmedrs397516376
geneviewrs397516376
scholarrs397516376
googlers397516376
pharmgkbrs397516376
gwascentralrs397516376
openSNPrs397516376
23andMers397516376
23andMe allrs397516376
SNP Nexus

SNPshotrs397516376
SNPdbers397516376
MSV3drs397516376
GWAS Ctlgrs397516376
Max Magnitude0
ClinVar
Risk rs397516376(T;T)
Alt rs397516376(T;T)
Reference rs397516376(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene TPM1
CLNDBN not specified
Reversed 0
HGVS NC_000015.9:g.63353123C>T
CLNSRC
CLNACC RCV000036342.4,