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rs869312104

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869312104(-;-)
Make rs869312104(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178739177
GeneTTN
is asnp
is mentioned by
dbSNPrs869312104
ebirs869312104
HLIrs869312104
Exacrs869312104
Varsomers869312104
Maprs869312104
PheGenIrs869312104
hapmaprs869312104
1000 genomesrs869312104
hgdprs869312104
ensemblrs869312104
gopubmedrs869312104
geneviewrs869312104
scholarrs869312104
googlers869312104
pharmgkbrs869312104
gwascentralrs869312104
openSNPrs869312104
23andMers869312104
23andMe allrs869312104
SNP Nexus

SNPshotrs869312104
SNPdbers869312104
MSV3drs869312104
GWAS Ctlgrs869312104
Max Magnitude0
ClinVar
Risk rs869312104(;)
Alt rs869312104(;)
Reference rs869312104(A;A)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179603904delT
CLNSRC
CLNACC RCV000209552.1,