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rs869312038

From SNPedia

Orientationminus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs869312038(-;-)
Make rs869312038(-;CA)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178740589
GeneTTN
is asnp
is mentioned by
dbSNPrs869312038
ebirs869312038
HLIrs869312038
Exacrs869312038
Varsomers869312038
Maprs869312038
PheGenIrs869312038
hapmaprs869312038
1000 genomesrs869312038
hgdprs869312038
ensemblrs869312038
gopubmedrs869312038
geneviewrs869312038
scholarrs869312038
googlers869312038
pharmgkbrs869312038
gwascentralrs869312038
openSNPrs869312038
23andMers869312038
23andMe allrs869312038
SNP Nexus

SNPshotrs869312038
SNPdbers869312038
MSV3drs869312038
GWAS Ctlgrs869312038
Max Magnitude0
ClinVar
Risk rs869312038(;)
Alt rs869312038(;)
Reference rs869312038(CA;CA)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179605316_179605317delTG
CLNSRC
CLNACC RCV000209509.1,