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rs730881078

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881078(A;C)
Make rs730881078(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55154031
GeneTNNI3
is asnp
is mentioned by
dbSNPrs730881078
ebirs730881078
HLIrs730881078
Exacrs730881078
Varsomers730881078
Maprs730881078
PheGenIrs730881078
hapmaprs730881078
1000 genomesrs730881078
hgdprs730881078
ensemblrs730881078
gopubmedrs730881078
geneviewrs730881078
scholarrs730881078
googlers730881078
pharmgkbrs730881078
gwascentralrs730881078
openSNPrs730881078
23andMers730881078
23andMe allrs730881078
SNP Nexus

SNPshotrs730881078
SNPdbers730881078
MSV3drs730881078
GWAS Ctlgrs730881078
Max Magnitude0
ClinVar
Risk rs730881078(C;C)
Alt rs730881078(C;C)
Reference rs730881078(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene TNNI3
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.55665399T>G
CLNSRC
CLNACC RCV000159237.1,