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rs104893823

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893823(A;A)
Make rs104893823(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position52451285
GeneTNNC1
is asnp
is mentioned by
dbSNPrs104893823
ebirs104893823
HLIrs104893823
Exacrs104893823
Varsomers104893823
Maprs104893823
PheGenIrs104893823
hapmaprs104893823
1000 genomesrs104893823
hgdprs104893823
ensemblrs104893823
gopubmedrs104893823
geneviewrs104893823
scholarrs104893823
googlers104893823
pharmgkbrs104893823
gwascentralrs104893823
openSNPrs104893823
23andMers104893823
23andMe allrs104893823
SNP Nexus

SNPshotrs104893823
SNPdbers104893823
MSV3drs104893823
GWAS Ctlgrs104893823
Max Magnitude0
OMIM191040
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104893823(A;A)
Alt rs104893823(A;A)
Reference rs104893823(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 1Z
Variation info
Gene TNNC1
CLNDBN Dilated cardiomyopathy 1Z
Reversed 1
HGVS NC_000003.11:g.52485301C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013254.22,