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rs869312042

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312042(-;-)
Make rs869312042(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178636124
GeneTTN
is asnp
is mentioned by
dbSNPrs869312042
ebirs869312042
HLIrs869312042
Exacrs869312042
Varsomers869312042
Maprs869312042
PheGenIrs869312042
hapmaprs869312042
1000 genomesrs869312042
hgdprs869312042
ensemblrs869312042
gopubmedrs869312042
geneviewrs869312042
scholarrs869312042
googlers869312042
pharmgkbrs869312042
gwascentralrs869312042
openSNPrs869312042
23andMers869312042
23andMe allrs869312042
SNP Nexus

SNPshotrs869312042
SNPdbers869312042
MSV3drs869312042
GWAS Ctlgrs869312042
Max Magnitude0
ClinVar
Risk rs869312042(;)
Alt rs869312042(;)
Reference rs869312042(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179500851delC
CLNSRC
CLNACC RCV000209690.1,