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rs730881061

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881061(A;G)
Make rs730881061(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position52451415
GeneTNNC1
is asnp
is mentioned by
dbSNPrs730881061
ebirs730881061
HLIrs730881061
Exacrs730881061
Varsomers730881061
Maprs730881061
PheGenIrs730881061
hapmaprs730881061
1000 genomesrs730881061
hgdprs730881061
ensemblrs730881061
gopubmedrs730881061
geneviewrs730881061
scholarrs730881061
googlers730881061
pharmgkbrs730881061
gwascentralrs730881061
openSNPrs730881061
23andMers730881061
23andMe allrs730881061
SNP Nexus

SNPshotrs730881061
SNPdbers730881061
MSV3drs730881061
GWAS Ctlgrs730881061
Max Magnitude0
ClinVar
Risk rs730881061(G;G)
Alt rs730881061(G;G)
Reference rs730881061(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene TNNC1
CLNDBN not specified
Reversed 1
HGVS NC_000003.11:g.52485431T>C
CLNSRC
CLNACC RCV000159200.2,