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rs730881058

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730881058(A;A)
Make rs730881058(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position52451799
GeneTNNC1
is asnp
is mentioned by
dbSNPrs730881058
ebirs730881058
HLIrs730881058
Exacrs730881058
Varsomers730881058
Maprs730881058
PheGenIrs730881058
hapmaprs730881058
1000 genomesrs730881058
hgdprs730881058
ensemblrs730881058
gopubmedrs730881058
geneviewrs730881058
scholarrs730881058
googlers730881058
pharmgkbrs730881058
gwascentralrs730881058
openSNPrs730881058
23andMers730881058
23andMe allrs730881058
SNP Nexus

SNPshotrs730881058
SNPdbers730881058
MSV3drs730881058
GWAS Ctlgrs730881058
Max Magnitude0
ClinVar
Risk rs730881058(A;A)
Alt rs730881058(A;A)
Reference rs730881058(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNC1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.52485815C>T
CLNSRC
CLNACC RCV000159195.1,