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rs869312074

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312074(A;A)
Make rs869312074(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178576922
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312074
ebirs869312074
HLIrs869312074
Exacrs869312074
Varsomers869312074
Maprs869312074
PheGenIrs869312074
hapmaprs869312074
1000 genomesrs869312074
hgdprs869312074
ensemblrs869312074
gopubmedrs869312074
geneviewrs869312074
scholarrs869312074
googlers869312074
pharmgkbrs869312074
gwascentralrs869312074
openSNPrs869312074
23andMers869312074
23andMe allrs869312074
SNP Nexus

SNPshotrs869312074
SNPdbers869312074
MSV3drs869312074
GWAS Ctlgrs869312074
Max Magnitude0
ClinVar
Risk rs869312074(A;A)
Alt rs869312074(A;A)
Reference rs869312074(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.179441649C>T
CLNSRC
CLNACC RCV000209713.1,