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rs869312048

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312048(A;A)
Make rs869312048(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178615418
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312048
ebirs869312048
HLIrs869312048
Exacrs869312048
Varsomers869312048
Maprs869312048
PheGenIrs869312048
hapmaprs869312048
1000 genomesrs869312048
hgdprs869312048
ensemblrs869312048
gopubmedrs869312048
geneviewrs869312048
scholarrs869312048
googlers869312048
pharmgkbrs869312048
gwascentralrs869312048
openSNPrs869312048
23andMers869312048
23andMe allrs869312048
SNP Nexus

SNPshotrs869312048
SNPdbers869312048
MSV3drs869312048
GWAS Ctlgrs869312048
Max Magnitude0
ClinVar
Risk rs869312048(A;A)
Alt rs869312048(A;A)
Reference rs869312048(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.179480145C>T
CLNSRC
CLNACC RCV000209744.1,