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rs869312075

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869312075(-;-)
Make rs869312075(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178576289
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312075
ebirs869312075
HLIrs869312075
Exacrs869312075
Varsomers869312075
Maprs869312075
PheGenIrs869312075
hapmaprs869312075
1000 genomesrs869312075
hgdprs869312075
ensemblrs869312075
gopubmedrs869312075
geneviewrs869312075
scholarrs869312075
googlers869312075
pharmgkbrs869312075
gwascentralrs869312075
openSNPrs869312075
23andMers869312075
23andMe allrs869312075
SNP Nexus

SNPshotrs869312075
SNPdbers869312075
MSV3drs869312075
GWAS Ctlgrs869312075
Max Magnitude0
ClinVar
Risk rs869312075(;)
Alt rs869312075(;)
Reference rs869312075(A;A)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179441016delT
CLNSRC
CLNACC RCV000209210.1,