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rs774604740

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs774604740(-;-)
Make rs774604740(-;T)
Make rs774604740(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178570016
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs774604740
ebirs774604740
HLIrs774604740
Exacrs774604740
Varsomers774604740
Maprs774604740
PheGenIrs774604740
hapmaprs774604740
1000 genomesrs774604740
hgdprs774604740
ensemblrs774604740
gopubmedrs774604740
geneviewrs774604740
scholarrs774604740
googlers774604740
pharmgkbrs774604740
gwascentralrs774604740
openSNPrs774604740
23andMers774604740
23andMe allrs774604740
SNP Nexus

SNPshotrs774604740
SNPdbers774604740
MSV3drs774604740
GWAS Ctlgrs774604740
Max Magnitude0
ClinVar
Risk rs774604740(T;T)
Alt rs774604740(T;T)
Reference rs774604740(;)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000002.11:g.179434744dupT
CLNSRC
CLNACC RCV000209488.1,