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rs869312062

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312062(A;A)
Make rs869312062(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178558492
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312062
ebirs869312062
HLIrs869312062
Exacrs869312062
Varsomers869312062
Maprs869312062
PheGenIrs869312062
hapmaprs869312062
1000 genomesrs869312062
hgdprs869312062
ensemblrs869312062
gopubmedrs869312062
geneviewrs869312062
scholarrs869312062
googlers869312062
pharmgkbrs869312062
gwascentralrs869312062
openSNPrs869312062
23andMers869312062
23andMe allrs869312062
SNP Nexus

SNPshotrs869312062
SNPdbers869312062
MSV3drs869312062
GWAS Ctlgrs869312062
Max Magnitude0
ClinVar
Risk rs869312062(A;A)
Alt rs869312062(A;A)
Reference rs869312062(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179423219C>T
CLNSRC
CLNACC RCV000209192.1,