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rs397516487

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516487(C;G)
Make rs397516487(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position63061781
GeneTPM1
is asnp
is mentioned by
dbSNPrs397516487
ebirs397516487
HLIrs397516487
Exacrs397516487
Varsomers397516487
Maprs397516487
PheGenIrs397516487
hapmaprs397516487
1000 genomesrs397516487
hgdprs397516487
ensemblrs397516487
gopubmedrs397516487
geneviewrs397516487
scholarrs397516487
googlers397516487
pharmgkbrs397516487
gwascentralrs397516487
openSNPrs397516487
23andMers397516487
23andMe allrs397516487
SNP Nexus

SNPshotrs397516487
SNPdbers397516487
MSV3drs397516487
GWAS Ctlgrs397516487
Max Magnitude0
ClinVar
Risk rs397516487(G;G)
Alt rs397516487(G;G)
Reference rs397516487(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene TPM1
CLNDBN not specified
Reversed 0
HGVS NC_000015.9:g.63353980C>G
CLNSRC ClinVar
CLNACC RCV000036630.3,