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rs869312070

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312070(A;A)
Make rs869312070(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178613938
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312070
ebirs869312070
HLIrs869312070
Exacrs869312070
Varsomers869312070
Maprs869312070
PheGenIrs869312070
hapmaprs869312070
1000 genomesrs869312070
hgdprs869312070
ensemblrs869312070
gopubmedrs869312070
geneviewrs869312070
scholarrs869312070
googlers869312070
pharmgkbrs869312070
gwascentralrs869312070
openSNPrs869312070
23andMers869312070
23andMe allrs869312070
SNP Nexus

SNPshotrs869312070
SNPdbers869312070
MSV3drs869312070
GWAS Ctlgrs869312070
Max Magnitude0
ClinVar
Risk rs869312070(A;A)
Alt rs869312070(A;A)
Reference rs869312070(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.179478665C>T
CLNSRC
CLNACC RCV000209019.1,