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rs730881085

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881085(C;G)
Make rs730881085(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55156622
GeneTNNI3
is asnp
is mentioned by
dbSNPrs730881085
ebirs730881085
HLIrs730881085
Exacrs730881085
Varsomers730881085
Maprs730881085
PheGenIrs730881085
hapmaprs730881085
1000 genomesrs730881085
hgdprs730881085
ensemblrs730881085
gopubmedrs730881085
geneviewrs730881085
scholarrs730881085
googlers730881085
pharmgkbrs730881085
gwascentralrs730881085
openSNPrs730881085
23andMers730881085
23andMe allrs730881085
SNP Nexus

SNPshotrs730881085
SNPdbers730881085
MSV3drs730881085
GWAS Ctlgrs730881085
Max Magnitude0
ClinVar
Risk rs730881085(G;G)
Alt rs730881085(G;G)
Reference rs730881085(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNI3
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.55667990G>C
CLNSRC
CLNACC RCV000159256.1,