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rs869312040

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312040(-;-)
Make rs869312040(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178706934
GeneTTN
is asnp
is mentioned by
dbSNPrs869312040
ebirs869312040
HLIrs869312040
Exacrs869312040
Varsomers869312040
Maprs869312040
PheGenIrs869312040
hapmaprs869312040
1000 genomesrs869312040
hgdprs869312040
ensemblrs869312040
gopubmedrs869312040
geneviewrs869312040
scholarrs869312040
googlers869312040
pharmgkbrs869312040
gwascentralrs869312040
openSNPrs869312040
23andMers869312040
23andMe allrs869312040
SNP Nexus

SNPshotrs869312040
SNPdbers869312040
MSV3drs869312040
GWAS Ctlgrs869312040
Max Magnitude0
ClinVar
Risk rs869312040(;)
Alt rs869312040(;)
Reference rs869312040(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179571661delC
CLNSRC
CLNACC RCV000208897.1,