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rs730881080

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881080(A;G)
Make rs730881080(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55151890
GeneTNNI3
is asnp
is mentioned by
dbSNPrs730881080
ebirs730881080
HLIrs730881080
Exacrs730881080
Varsomers730881080
Maprs730881080
PheGenIrs730881080
hapmaprs730881080
1000 genomesrs730881080
hgdprs730881080
ensemblrs730881080
gopubmedrs730881080
geneviewrs730881080
scholarrs730881080
googlers730881080
pharmgkbrs730881080
gwascentralrs730881080
openSNPrs730881080
23andMers730881080
23andMe allrs730881080
SNP Nexus

SNPshotrs730881080
SNPdbers730881080
MSV3drs730881080
GWAS Ctlgrs730881080
Max Magnitude0
ClinVar
Risk rs730881080(G;G)
Alt rs730881080(G;G)
Reference rs730881080(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene TNNI3
CLNDBN not specified
Reversed 1
HGVS NC_000019.9:g.55663258T>C
CLNSRC
CLNACC RCV000159243.2,