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rs876661394

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876661394(C;T)
Make rs876661394(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position55154056
GeneTNNI3
is asnp
is mentioned by
dbSNPrs876661394
ebirs876661394
HLIrs876661394
Exacrs876661394
Varsomers876661394
Maprs876661394
PheGenIrs876661394
hapmaprs876661394
1000 genomesrs876661394
hgdprs876661394
ensemblrs876661394
gopubmedrs876661394
geneviewrs876661394
scholarrs876661394
googlers876661394
pharmgkbrs876661394
gwascentralrs876661394
openSNPrs876661394
23andMers876661394
23andMe allrs876661394
SNP Nexus

SNPshotrs876661394
SNPdbers876661394
MSV3drs876661394
GWAS Ctlgrs876661394
Max Magnitude0
ClinVar
Risk rs876661394(T;T)
Alt rs876661394(T;T)
Reference rs876661394(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNI3
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.55665424G>A
CLNSRC
CLNACC RCV000223834.1,