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rs730881089

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881089(A;T)
Make rs730881089(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55151914
GeneTNNI3
is asnp
is mentioned by
dbSNPrs730881089
ebirs730881089
HLIrs730881089
Exacrs730881089
Varsomers730881089
Maprs730881089
PheGenIrs730881089
hapmaprs730881089
1000 genomesrs730881089
hgdprs730881089
ensemblrs730881089
gopubmedrs730881089
geneviewrs730881089
scholarrs730881089
googlers730881089
pharmgkbrs730881089
gwascentralrs730881089
openSNPrs730881089
23andMers730881089
23andMe allrs730881089
SNP Nexus

SNPshotrs730881089
SNPdbers730881089
MSV3drs730881089
GWAS Ctlgrs730881089
Max Magnitude0
ClinVar
Risk rs730881089(T;T)
Alt rs730881089(T;T)
Reference rs730881089(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNI3
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.55663282T>A
CLNSRC
CLNACC RCV000159260.1,