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rs368452607

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs368452607(G;T)
Make rs368452607(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178588700
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs368452607
ebirs368452607
HLIrs368452607
Exacrs368452607
Varsomers368452607
Maprs368452607
PheGenIrs368452607
hapmaprs368452607
1000 genomesrs368452607
hgdprs368452607
ensemblrs368452607
gopubmedrs368452607
geneviewrs368452607
scholarrs368452607
googlers368452607
pharmgkbrs368452607
gwascentralrs368452607
openSNPrs368452607
23andMers368452607
23andMe allrs368452607
SNP Nexus

SNPshotrs368452607
SNPdbers368452607
MSV3drs368452607
GWAS Ctlgrs368452607
Max Magnitude0
ClinVar
Risk rs368452607(T;T)
Alt rs368452607(T;T)
Reference rs368452607(G;G)
Significance Pathogenic
Disease not provided Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN not provided Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000002.11:g.179453427G>A
CLNSRC
CLNACC RCV000184387.1, RCV000209637.1,