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rs730881086

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881086(A;A)
Make rs730881086(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55156603
GeneTNNI3
is asnp
is mentioned by
dbSNPrs730881086
ebirs730881086
HLIrs730881086
Exacrs730881086
Varsomers730881086
Maprs730881086
PheGenIrs730881086
hapmaprs730881086
1000 genomesrs730881086
hgdprs730881086
ensemblrs730881086
gopubmedrs730881086
geneviewrs730881086
scholarrs730881086
googlers730881086
pharmgkbrs730881086
gwascentralrs730881086
openSNPrs730881086
23andMers730881086
23andMe allrs730881086
SNP Nexus

SNPshotrs730881086
SNPdbers730881086
MSV3drs730881086
GWAS Ctlgrs730881086
Max Magnitude0
ClinVar
Risk rs730881086(A;A)
Alt rs730881086(A;A)
Reference rs730881086(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNI3
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.55667971C>T
CLNSRC
CLNACC RCV000159257.1,