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rs730881059

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730881059(A;A)
Make rs730881059(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position52451771
GeneTNNC1
is asnp
is mentioned by
dbSNPrs730881059
ebirs730881059
HLIrs730881059
Exacrs730881059
Varsomers730881059
Maprs730881059
PheGenIrs730881059
hapmaprs730881059
1000 genomesrs730881059
hgdprs730881059
ensemblrs730881059
gopubmedrs730881059
geneviewrs730881059
scholarrs730881059
googlers730881059
pharmgkbrs730881059
gwascentralrs730881059
openSNPrs730881059
23andMers730881059
23andMe allrs730881059
SNP Nexus

SNPshotrs730881059
SNPdbers730881059
MSV3drs730881059
GWAS Ctlgrs730881059
Max Magnitude0
ClinVar
Risk rs730881059(A;A)
Alt rs730881059(A;A)
Reference rs730881059(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNC1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.52485787A>T
CLNSRC
CLNACC RCV000159196.1,