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rs730881066

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881066(A;T)
Make rs730881066(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55156639
GeneTNNI3
is asnp
is mentioned by
dbSNPrs730881066
ebirs730881066
HLIrs730881066
Exacrs730881066
Varsomers730881066
Maprs730881066
PheGenIrs730881066
hapmaprs730881066
1000 genomesrs730881066
hgdprs730881066
ensemblrs730881066
gopubmedrs730881066
geneviewrs730881066
scholarrs730881066
googlers730881066
pharmgkbrs730881066
gwascentralrs730881066
openSNPrs730881066
23andMers730881066
23andMe allrs730881066
SNP Nexus

SNPshotrs730881066
SNPdbers730881066
MSV3drs730881066
GWAS Ctlgrs730881066
Max Magnitude0
ClinVar
Risk rs730881066(T;T)
Alt rs730881066(T;T)
Reference rs730881066(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNI3
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.55668007T>A
CLNSRC
CLNACC RCV000159209.1,