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rs869025556

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869025556(-;-)
Make rs869025556(-;A)
Make rs869025556(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178740362
GeneTTN
is asnp
is mentioned by
dbSNPrs869025556
ebirs869025556
HLIrs869025556
Exacrs869025556
Varsomers869025556
Maprs869025556
PheGenIrs869025556
hapmaprs869025556
1000 genomesrs869025556
hgdprs869025556
ensemblrs869025556
gopubmedrs869025556
geneviewrs869025556
scholarrs869025556
googlers869025556
pharmgkbrs869025556
gwascentralrs869025556
openSNPrs869025556
23andMers869025556
23andMe allrs869025556
SNP Nexus

SNPshotrs869025556
SNPdbers869025556
MSV3drs869025556
GWAS Ctlgrs869025556
Max Magnitude0
ClinVar
Risk rs869025556(A;A)
Alt rs869025556(A;A)
Reference rs869025556(;)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179605090dupT
CLNSRC
CLNACC RCV000207997.1,