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

rs730881090

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881090(C;G)
Make rs730881090(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55151885
GeneTNNI3
is asnp
is mentioned by
dbSNPrs730881090
ebirs730881090
HLIrs730881090
Exacrs730881090
Varsomers730881090
Maprs730881090
PheGenIrs730881090
hapmaprs730881090
1000 genomesrs730881090
hgdprs730881090
ensemblrs730881090
gopubmedrs730881090
geneviewrs730881090
scholarrs730881090
googlers730881090
pharmgkbrs730881090
gwascentralrs730881090
openSNPrs730881090
23andMers730881090
23andMe allrs730881090
SNP Nexus

SNPshotrs730881090
SNPdbers730881090
MSV3drs730881090
GWAS Ctlgrs730881090
Max Magnitude0
ClinVar
Risk rs730881090(G;G)
Alt rs730881090(G;G)
Reference rs730881090(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TNNI3
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.55663253G>C
CLNSRC
CLNACC RCV000159261.2,