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rs767450912

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs767450912(A;A)
Make rs767450912(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178569415
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs767450912
ebirs767450912
HLIrs767450912
Exacrs767450912
Varsomers767450912
Maprs767450912
PheGenIrs767450912
hapmaprs767450912
1000 genomesrs767450912
hgdprs767450912
ensemblrs767450912
gopubmedrs767450912
geneviewrs767450912
scholarrs767450912
googlers767450912
pharmgkbrs767450912
gwascentralrs767450912
openSNPrs767450912
23andMers767450912
23andMe allrs767450912
SNP Nexus

SNPshotrs767450912
SNPdbers767450912
MSV3drs767450912
GWAS Ctlgrs767450912
Max Magnitude0
ClinVar
Risk rs767450912(A,T;A,T)
Alt rs767450912(A,T;A,T)
Reference rs767450912(G;G)
Significance Probable-Pathogenic
Disease Dilated cardiomyopathy 1G
Variation info
Gene TTN TTN-AS1
CLNDBN Dilated cardiomyopathy 1G
Reversed 0
HGVS NC_000002.11:g.179434142G>A
CLNSRC
CLNACC RCV000230707.1,