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rs869025550

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869025550(A;G)
Make rs869025550(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178579395
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869025550
ebirs869025550
HLIrs869025550
Exacrs869025550
Varsomers869025550
Maprs869025550
PheGenIrs869025550
hapmaprs869025550
1000 genomesrs869025550
hgdprs869025550
ensemblrs869025550
gopubmedrs869025550
geneviewrs869025550
scholarrs869025550
googlers869025550
pharmgkbrs869025550
gwascentralrs869025550
openSNPrs869025550
23andMers869025550
23andMe allrs869025550
SNP Nexus

SNPshotrs869025550
SNPdbers869025550
MSV3drs869025550
GWAS Ctlgrs869025550
Max Magnitude0
ClinVar
Risk rs869025550(G;G)
Alt rs869025550(G;G)
Reference rs869025550(A;A)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179444122T>C
CLNSRC
CLNACC RCV000208534.1,