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rs869312120

From SNPedia

Orientationminus
Geno Mag Summary
(ACTT;ACTT) 0 common in clinvar
Make rs869312120(-;-)
Make rs869312120(-;ACTT)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178557372
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312120
ebirs869312120
HLIrs869312120
Exacrs869312120
Varsomers869312120
Maprs869312120
PheGenIrs869312120
hapmaprs869312120
1000 genomesrs869312120
hgdprs869312120
ensemblrs869312120
gopubmedrs869312120
geneviewrs869312120
scholarrs869312120
googlers869312120
pharmgkbrs869312120
gwascentralrs869312120
openSNPrs869312120
23andMers869312120
23andMe allrs869312120
SNP Nexus

SNPshotrs869312120
SNPdbers869312120
MSV3drs869312120
GWAS Ctlgrs869312120
Max Magnitude0
ClinVar
Risk rs869312120(;)
Alt rs869312120(;)
Reference rs869312120(ACTT;ACTT)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179422099_179422102delAAGT
CLNSRC
CLNACC RCV000208914.1,