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rs730881068

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881068(C;T)
Make rs730881068(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55154821
GeneTNNI3
is asnp
is mentioned by
dbSNPrs730881068
ebirs730881068
HLIrs730881068
Exacrs730881068
Varsomers730881068
Maprs730881068
PheGenIrs730881068
hapmaprs730881068
1000 genomesrs730881068
hgdprs730881068
ensemblrs730881068
gopubmedrs730881068
geneviewrs730881068
scholarrs730881068
googlers730881068
pharmgkbrs730881068
gwascentralrs730881068
openSNPrs730881068
23andMers730881068
23andMe allrs730881068
SNP Nexus

SNPshotrs730881068
SNPdbers730881068
MSV3drs730881068
GWAS Ctlgrs730881068
Max Magnitude0
ClinVar
Risk rs730881068(G,T;G,T)
Alt rs730881068(G,T;G,T)
Reference rs730881068(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene TNNI3
CLNDBN not specified
Reversed 1
HGVS NC_000019.9:g.55666189G>A
CLNSRC
CLNACC RCV000159212.2,