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

rs869312103

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312103(G;T)
Make rs869312103(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178739333
GeneTTN
is asnp
is mentioned by
dbSNPrs869312103
ebirs869312103
HLIrs869312103
Exacrs869312103
Varsomers869312103
Maprs869312103
PheGenIrs869312103
hapmaprs869312103
1000 genomesrs869312103
hgdprs869312103
ensemblrs869312103
gopubmedrs869312103
geneviewrs869312103
scholarrs869312103
googlers869312103
pharmgkbrs869312103
gwascentralrs869312103
openSNPrs869312103
23andMers869312103
23andMe allrs869312103
SNP Nexus

SNPshotrs869312103
SNPdbers869312103
MSV3drs869312103
GWAS Ctlgrs869312103
Max Magnitude0
ClinVar
Risk rs869312103(T;T)
Alt rs869312103(T;T)
Reference rs869312103(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179604060C>A
CLNSRC
CLNACC RCV000209226.1,