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rs730881075

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881075(C;G)
Make rs730881075(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55154065
GeneTNNI3
is asnp
is mentioned by
dbSNPrs730881075
dbSNP (old)rs730881075
ClinGenrs730881075
ebirs730881075
HLIrs730881075
Exacrs730881075
Gnomadrs730881075
Varsomers730881075
Maprs730881075
PheGenIrs730881075
Biobankrs730881075
1000 genomesrs730881075
hgdprs730881075
ensemblrs730881075
gopubmedrs730881075
geneviewrs730881075
scholarrs730881075
googlers730881075
pharmgkbrs730881075
gwascentralrs730881075
openSNPrs730881075
23andMers730881075
23andMe allrs730881075
SNP Nexus

SNPshotrs730881075
SNPdbers730881075
MSV3drs730881075
GWAS Ctlgrs730881075
Max Magnitude0
ClinVar
Risk rs730881075(G;G)
Alt rs730881075(G;G)
Reference Rs730881075(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNI3
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.55665433G>C
CLNSRC
CLNACC RCV000159233.2,