Have questions? Visit https://www.reddit.com/r/SNPedia

rs763824247

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs763824247(C;T)
Make rs763824247(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178583706
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs763824247
ebirs763824247
HLIrs763824247
Exacrs763824247
Varsomers763824247
Maprs763824247
PheGenIrs763824247
hapmaprs763824247
1000 genomesrs763824247
hgdprs763824247
ensemblrs763824247
gopubmedrs763824247
geneviewrs763824247
scholarrs763824247
googlers763824247
pharmgkbrs763824247
gwascentralrs763824247
openSNPrs763824247
23andMers763824247
23andMe allrs763824247
SNP Nexus

SNPshotrs763824247
SNPdbers763824247
MSV3drs763824247
GWAS Ctlgrs763824247
Max Magnitude0
ClinVar
Risk rs763824247(T;T)
Alt rs763824247(T;T)
Reference rs763824247(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000002.11:g.179448433C>A
CLNSRC
CLNACC RCV000209781.1,