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rs869025544

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025544(A;A)
Make rs869025544(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178594134
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869025544
ebirs869025544
HLIrs869025544
Exacrs869025544
Varsomers869025544
Maprs869025544
PheGenIrs869025544
hapmaprs869025544
1000 genomesrs869025544
hgdprs869025544
ensemblrs869025544
gopubmedrs869025544
geneviewrs869025544
scholarrs869025544
googlers869025544
pharmgkbrs869025544
gwascentralrs869025544
openSNPrs869025544
23andMers869025544
23andMe allrs869025544
SNP Nexus

SNPshotrs869025544
SNPdbers869025544
MSV3drs869025544
GWAS Ctlgrs869025544
Max Magnitude0
ClinVar
Risk rs869025544(A;A)
Alt rs869025544(A;A)
Reference rs869025544(G;G)
Significance Probable-Pathogenic
Disease Left ventricular noncompaction cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Left ventricular noncompaction cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179458861C>T
CLNSRC
CLNACC RCV000208156.1,