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rs869312106

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869312106(-;-)
Make rs869312106(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178633863
GeneTTN
is asnp
is mentioned by
dbSNPrs869312106
ebirs869312106
HLIrs869312106
Exacrs869312106
Varsomers869312106
Maprs869312106
PheGenIrs869312106
hapmaprs869312106
1000 genomesrs869312106
hgdprs869312106
ensemblrs869312106
gopubmedrs869312106
geneviewrs869312106
scholarrs869312106
googlers869312106
pharmgkbrs869312106
gwascentralrs869312106
openSNPrs869312106
23andMers869312106
23andMe allrs869312106
SNP Nexus

SNPshotrs869312106
SNPdbers869312106
MSV3drs869312106
GWAS Ctlgrs869312106
Max Magnitude0
ClinVar
Risk rs869312106(;)
Alt rs869312106(;)
Reference rs869312106(A;A)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179498590delT
CLNSRC
CLNACC RCV000209251.1,