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rs786205398

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205398(A;A)
Make rs786205398(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178682696
GeneTTN
is asnp
is mentioned by
dbSNPrs786205398
ebirs786205398
HLIrs786205398
Exacrs786205398
Varsomers786205398
Maprs786205398
PheGenIrs786205398
hapmaprs786205398
1000 genomesrs786205398
hgdprs786205398
ensemblrs786205398
gopubmedrs786205398
geneviewrs786205398
scholarrs786205398
googlers786205398
pharmgkbrs786205398
gwascentralrs786205398
openSNPrs786205398
23andMers786205398
23andMe allrs786205398
SNP Nexus

SNPshotrs786205398
SNPdbers786205398
MSV3drs786205398
GWAS Ctlgrs786205398
Max Magnitude0
ClinVar
Risk rs786205398(A;A)
Alt rs786205398(A;A)
Reference rs786205398(G;G)
Significance Probable-Pathogenic
Disease Dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179547423C>T
CLNSRC
CLNACC RCV000171846.1,