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rs730881077

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881077(A;G)
Make rs730881077(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55154032
GeneTNNI3
is asnp
is mentioned by
dbSNPrs730881077
ebirs730881077
HLIrs730881077
Exacrs730881077
Varsomers730881077
Maprs730881077
PheGenIrs730881077
hapmaprs730881077
1000 genomesrs730881077
hgdprs730881077
ensemblrs730881077
gopubmedrs730881077
geneviewrs730881077
scholarrs730881077
googlers730881077
pharmgkbrs730881077
gwascentralrs730881077
openSNPrs730881077
23andMers730881077
23andMe allrs730881077
SNP Nexus

SNPshotrs730881077
SNPdbers730881077
MSV3drs730881077
GWAS Ctlgrs730881077
Max Magnitude0
ClinVar
Risk rs730881077(G;G)
Alt rs730881077(G;G)
Reference rs730881077(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene TNNI3
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.55665400T>C
CLNSRC
CLNACC RCV000159236.1,