Have questions? Visit https://www.reddit.com/r/SNPedia

rs397516387

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516387(C;T)
Make rs397516387(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position63062598
GeneTPM1
is asnp
is mentioned by
dbSNPrs397516387
ebirs397516387
HLIrs397516387
Exacrs397516387
Varsomers397516387
Maprs397516387
PheGenIrs397516387
hapmaprs397516387
1000 genomesrs397516387
hgdprs397516387
ensemblrs397516387
gopubmedrs397516387
geneviewrs397516387
scholarrs397516387
googlers397516387
pharmgkbrs397516387
gwascentralrs397516387
openSNPrs397516387
23andMers397516387
23andMe allrs397516387
SNP Nexus

SNPshotrs397516387
SNPdbers397516387
MSV3drs397516387
GWAS Ctlgrs397516387
Max Magnitude0
ClinVar
Risk rs397516387(T;T)
Alt rs397516387(T;T)
Reference rs397516387(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene TPM1
CLNDBN not specified
Reversed 0
HGVS NC_000015.9:g.63354797C>T
CLNSRC ClinVar
CLNACC RCV000036357.4,