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rs876661393

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876661393(A;A)
Make rs876661393(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position52452147
GeneTNNC1
is asnp
is mentioned by
dbSNPrs876661393
dbSNP (classic)rs876661393
ClinGenrs876661393
ebirs876661393
HLIrs876661393
Exacrs876661393
Gnomadrs876661393
Varsomers876661393
LitVarrs876661393
Maprs876661393
PheGenIrs876661393
Biobankrs876661393
1000 genomesrs876661393
hgdprs876661393
ensemblrs876661393
geneviewrs876661393
scholarrs876661393
googlers876661393
pharmgkbrs876661393
gwascentralrs876661393
openSNPrs876661393
23andMers876661393
SNPshotrs876661393
SNPdbers876661393
MSV3drs876661393
GWAS Ctlgrs876661393
Max Magnitude0
ClinVar
Risk rs876661393(A;A)
Alt rs876661393(A;A)
Reference Rs876661393(C;C)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene TNNC1
CLNDBN not specified not provided
Reversed 1
HGVS NC_000003.11:g.52486163G>T
CLNSRC
CLNACC RCV000223755.1, RCV000483835.1,