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rs730881081

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881081(A;G)
Make rs730881081(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55151886
GeneTNNI3
is asnp
is mentioned by
dbSNPrs730881081
ebirs730881081
HLIrs730881081
Exacrs730881081
Varsomers730881081
Maprs730881081
PheGenIrs730881081
hapmaprs730881081
1000 genomesrs730881081
hgdprs730881081
ensemblrs730881081
gopubmedrs730881081
geneviewrs730881081
scholarrs730881081
googlers730881081
pharmgkbrs730881081
gwascentralrs730881081
openSNPrs730881081
23andMers730881081
23andMe allrs730881081
SNP Nexus

SNPshotrs730881081
SNPdbers730881081
MSV3drs730881081
GWAS Ctlgrs730881081
Max Magnitude0
ClinVar
Risk rs730881081(C,G;C,G)
Alt rs730881081(C,G;C,G)
Reference rs730881081(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNI3
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.55663254T>C
CLNSRC
CLNACC RCV000159245.1,