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rs869312043

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312043(C;T)
Make rs869312043(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178636098
GeneTTN
is asnp
is mentioned by
dbSNPrs869312043
ebirs869312043
HLIrs869312043
Exacrs869312043
Varsomers869312043
Maprs869312043
PheGenIrs869312043
hapmaprs869312043
1000 genomesrs869312043
hgdprs869312043
ensemblrs869312043
gopubmedrs869312043
geneviewrs869312043
scholarrs869312043
googlers869312043
pharmgkbrs869312043
gwascentralrs869312043
openSNPrs869312043
23andMers869312043
23andMe allrs869312043
SNP Nexus

SNPshotrs869312043
SNPdbers869312043
MSV3drs869312043
GWAS Ctlgrs869312043
Max Magnitude0
ClinVar
Risk rs869312043(T;T)
Alt rs869312043(T;T)
Reference rs869312043(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179500825G>A
CLNSRC
CLNACC RCV000209073.1,