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rs886039440

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039440(G;T)
Make rs886039440(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome3
Position52452167
GeneTNNC1
is asnp
is mentioned by
dbSNPrs886039440
dbSNP (classic)rs886039440
ClinGenrs886039440
ebirs886039440
HLIrs886039440
Exacrs886039440
Gnomadrs886039440
Varsomers886039440
LitVarrs886039440
Maprs886039440
PheGenIrs886039440
Biobankrs886039440
1000 genomesrs886039440
hgdprs886039440
ensemblrs886039440
geneviewrs886039440
scholarrs886039440
googlers886039440
pharmgkbrs886039440
gwascentralrs886039440
openSNPrs886039440
23andMers886039440
SNPshotrs886039440
SNPdbers886039440
MSV3drs886039440
GWAS Ctlgrs886039440
Max Magnitude0
ClinVar
Risk rs886039440(T;T)
Alt rs886039440(T;T)
Reference Rs886039440(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNC1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.52486183C>A
CLNSRC
CLNACC RCV000255337.1,