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rs869312044

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312044(-;-)
Make rs869312044(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178631256
GeneTTN
is asnp
is mentioned by
dbSNPrs869312044
ebirs869312044
HLIrs869312044
Exacrs869312044
Varsomers869312044
Maprs869312044
PheGenIrs869312044
hapmaprs869312044
1000 genomesrs869312044
hgdprs869312044
ensemblrs869312044
gopubmedrs869312044
geneviewrs869312044
scholarrs869312044
googlers869312044
pharmgkbrs869312044
gwascentralrs869312044
openSNPrs869312044
23andMers869312044
23andMe allrs869312044
SNP Nexus

SNPshotrs869312044
SNPdbers869312044
MSV3drs869312044
GWAS Ctlgrs869312044
Max Magnitude0
ClinVar
Risk rs869312044(;)
Alt rs869312044(;)
Reference rs869312044(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179495983delC
CLNSRC
CLNACC RCV000209396.1,