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

rs397516382

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516382(A;A)
Make rs397516382(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position63042893
GeneTPM1
is asnp
is mentioned by
dbSNPrs397516382
ebirs397516382
HLIrs397516382
Exacrs397516382
Varsomers397516382
Maprs397516382
PheGenIrs397516382
hapmaprs397516382
1000 genomesrs397516382
hgdprs397516382
ensemblrs397516382
gopubmedrs397516382
geneviewrs397516382
scholarrs397516382
googlers397516382
pharmgkbrs397516382
gwascentralrs397516382
openSNPrs397516382
23andMers397516382
23andMe allrs397516382
SNP Nexus

SNPshotrs397516382
SNPdbers397516382
MSV3drs397516382
GWAS Ctlgrs397516382
Max Magnitude0
ClinVar
Risk rs397516382(A;A)
Alt rs397516382(A;A)
Reference rs397516382(G;G)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene TPM1
CLNDBN not specified not provided
Reversed 0
HGVS NC_000015.9:g.63335092G>A
CLNSRC
CLNACC RCV000036351.4, RCV000223842.1,