Have questions? Visit https://www.reddit.com/r/SNPedia

rs869312046

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869312046(G;G)
Make rs869312046(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178620798
GeneTTN
is asnp
is mentioned by
dbSNPrs869312046
ebirs869312046
HLIrs869312046
Exacrs869312046
Varsomers869312046
Maprs869312046
PheGenIrs869312046
hapmaprs869312046
1000 genomesrs869312046
hgdprs869312046
ensemblrs869312046
gopubmedrs869312046
geneviewrs869312046
scholarrs869312046
googlers869312046
pharmgkbrs869312046
gwascentralrs869312046
openSNPrs869312046
23andMers869312046
23andMe allrs869312046
SNP Nexus

SNPshotrs869312046
SNPdbers869312046
MSV3drs869312046
GWAS Ctlgrs869312046
Max Magnitude0
ClinVar
Risk rs869312046(G;G)
Alt rs869312046(G;G)
Reference rs869312046(T;T)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179485525A>C
CLNSRC
CLNACC RCV000209593.1,