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rs730881076

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881076(A;C)
Make rs730881076(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55154058
GeneTNNI3
is asnp
is mentioned by
dbSNPrs730881076
ebirs730881076
HLIrs730881076
Exacrs730881076
Varsomers730881076
Maprs730881076
PheGenIrs730881076
hapmaprs730881076
1000 genomesrs730881076
hgdprs730881076
ensemblrs730881076
gopubmedrs730881076
geneviewrs730881076
scholarrs730881076
googlers730881076
pharmgkbrs730881076
gwascentralrs730881076
openSNPrs730881076
23andMers730881076
23andMe allrs730881076
SNP Nexus

SNPshotrs730881076
SNPdbers730881076
MSV3drs730881076
GWAS Ctlgrs730881076
Max Magnitude0
ClinVar
Risk rs730881076(C;C)
Alt rs730881076(C;C)
Reference rs730881076(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNI3
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.55665426T>G
CLNSRC
CLNACC RCV000159234.2,