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rs730881062

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730881062(A;G)
Make rs730881062(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position52451399
GeneTNNC1
is asnp
is mentioned by
dbSNPrs730881062
ebirs730881062
HLIrs730881062
Exacrs730881062
Varsomers730881062
Maprs730881062
PheGenIrs730881062
hapmaprs730881062
1000 genomesrs730881062
hgdprs730881062
ensemblrs730881062
gopubmedrs730881062
geneviewrs730881062
scholarrs730881062
googlers730881062
pharmgkbrs730881062
gwascentralrs730881062
openSNPrs730881062
23andMers730881062
23andMe allrs730881062
SNP Nexus

SNPshotrs730881062
SNPdbers730881062
MSV3drs730881062
GWAS Ctlgrs730881062
Max Magnitude0
ClinVar
Risk rs730881062(G;G)
Alt rs730881062(G;G)
Reference rs730881062(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNC1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.52485415T>C
CLNSRC
CLNACC RCV000159201.2,