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rs730881088

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881088(A;G)
Make rs730881088(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55154782
GeneTNNI3
is asnp
is mentioned by
dbSNPrs730881088
ebirs730881088
HLIrs730881088
Exacrs730881088
Varsomers730881088
Maprs730881088
PheGenIrs730881088
hapmaprs730881088
1000 genomesrs730881088
hgdprs730881088
ensemblrs730881088
gopubmedrs730881088
geneviewrs730881088
scholarrs730881088
googlers730881088
pharmgkbrs730881088
gwascentralrs730881088
openSNPrs730881088
23andMers730881088
23andMe allrs730881088
SNP Nexus

SNPshotrs730881088
SNPdbers730881088
MSV3drs730881088
GWAS Ctlgrs730881088
Max Magnitude0
ClinVar
Risk rs730881088(G;G)
Alt rs730881088(G;G)
Reference rs730881088(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene TNNI3
CLNDBN not specified
Reversed 1
HGVS NC_000019.9:g.55666150T>C
CLNSRC
CLNACC RCV000159259.2,