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rs730881065

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881065(C;G)
Make rs730881065(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position52452153
GeneTNNC1
is asnp
is mentioned by
dbSNPrs730881065
ebirs730881065
HLIrs730881065
Exacrs730881065
Varsomers730881065
Maprs730881065
PheGenIrs730881065
hapmaprs730881065
1000 genomesrs730881065
hgdprs730881065
ensemblrs730881065
gopubmedrs730881065
geneviewrs730881065
scholarrs730881065
googlers730881065
pharmgkbrs730881065
gwascentralrs730881065
openSNPrs730881065
23andMers730881065
23andMe allrs730881065
SNP Nexus

SNPshotrs730881065
SNPdbers730881065
MSV3drs730881065
GWAS Ctlgrs730881065
Max Magnitude0
ClinVar
Risk rs730881065(G;G)
Alt rs730881065(G;G)
Reference rs730881065(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNC1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.52486169G>C
CLNSRC
CLNACC RCV000159206.1,