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

rs730881072

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881072(A;A)
Make rs730881072(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55154128
GeneTNNI3
is asnp
is mentioned by
dbSNPrs730881072
ClinGenrs730881072
ebirs730881072
HLIrs730881072
Exacrs730881072
Varsomers730881072
Maprs730881072
PheGenIrs730881072
Biobankrs730881072
1000 genomesrs730881072
hgdprs730881072
ensemblrs730881072
gopubmedrs730881072
geneviewrs730881072
scholarrs730881072
googlers730881072
pharmgkbrs730881072
gwascentralrs730881072
openSNPrs730881072
23andMers730881072
23andMe allrs730881072
SNP Nexus

SNPshotrs730881072
SNPdbers730881072
MSV3drs730881072
GWAS Ctlgrs730881072
Max Magnitude0
ClinVar
Risk rs730881072(A;A)
Alt rs730881072(A;A)
Reference Rs730881072(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNI3
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.55665496C>T
CLNSRC
CLNACC RCV000159224.2,