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rs730881079

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881079(A;G)
Make rs730881079(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55151913
GeneTNNI3
is asnp
is mentioned by
dbSNPrs730881079
ebirs730881079
HLIrs730881079
Exacrs730881079
Varsomers730881079
Maprs730881079
PheGenIrs730881079
hapmaprs730881079
1000 genomesrs730881079
hgdprs730881079
ensemblrs730881079
gopubmedrs730881079
geneviewrs730881079
scholarrs730881079
googlers730881079
pharmgkbrs730881079
gwascentralrs730881079
openSNPrs730881079
23andMers730881079
23andMe allrs730881079
SNP Nexus

SNPshotrs730881079
SNPdbers730881079
MSV3drs730881079
GWAS Ctlgrs730881079
Max Magnitude0
ClinVar
Risk rs730881079(G;G)
Alt rs730881079(G;G)
Reference rs730881079(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNI3
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.55663281T>C
CLNSRC
CLNACC RCV000159238.2,