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rs869312105

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869312105(G;G)
Make rs869312105(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178635489
GeneTTN
is asnp
is mentioned by
dbSNPrs869312105
ebirs869312105
HLIrs869312105
Exacrs869312105
Varsomers869312105
Maprs869312105
PheGenIrs869312105
hapmaprs869312105
1000 genomesrs869312105
hgdprs869312105
ensemblrs869312105
gopubmedrs869312105
geneviewrs869312105
scholarrs869312105
googlers869312105
pharmgkbrs869312105
gwascentralrs869312105
openSNPrs869312105
23andMers869312105
23andMe allrs869312105
SNP Nexus

SNPshotrs869312105
SNPdbers869312105
MSV3drs869312105
GWAS Ctlgrs869312105
Max Magnitude0
ClinVar
Risk rs869312105(G;G)
Alt rs869312105(G;G)
Reference rs869312105(T;T)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179500216A>C
CLNSRC
CLNACC RCV000208928.1,