Have questions? Visit https://www.reddit.com/r/SNPedia

rs730881087

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881087(A;G)
Make rs730881087(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55154811
GeneTNNI3
is asnp
is mentioned by
dbSNPrs730881087
ebirs730881087
HLIrs730881087
Exacrs730881087
Varsomers730881087
Maprs730881087
PheGenIrs730881087
hapmaprs730881087
1000 genomesrs730881087
hgdprs730881087
ensemblrs730881087
gopubmedrs730881087
geneviewrs730881087
scholarrs730881087
googlers730881087
pharmgkbrs730881087
gwascentralrs730881087
openSNPrs730881087
23andMers730881087
23andMe allrs730881087
SNP Nexus

SNPshotrs730881087
SNPdbers730881087
MSV3drs730881087
GWAS Ctlgrs730881087
Max Magnitude0
ClinVar
Risk rs730881087(G;G)
Alt rs730881087(G;G)
Reference rs730881087(A;A)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene TNNI3
CLNDBN not provided not specified
Reversed 1
HGVS NC_000019.9:g.55666179T>C
CLNSRC
CLNACC RCV000159258.1, RCV000223790.1,