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

rs730880244

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880244(A;C)
Make rs730880244(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178635717
GeneTTN
is asnp
is mentioned by
dbSNPrs730880244
ebirs730880244
HLIrs730880244
Exacrs730880244
Varsomers730880244
Maprs730880244
PheGenIrs730880244
hapmaprs730880244
1000 genomesrs730880244
hgdprs730880244
ensemblrs730880244
gopubmedrs730880244
geneviewrs730880244
scholarrs730880244
googlers730880244
pharmgkbrs730880244
gwascentralrs730880244
openSNPrs730880244
23andMers730880244
23andMe allrs730880244
SNP Nexus

SNPshotrs730880244
SNPdbers730880244
MSV3drs730880244
GWAS Ctlgrs730880244
Max Magnitude0
ClinVar
Risk rs730880244(C;C)
Alt rs730880244(C;C)
Reference rs730880244(A;A)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179500444T>G
CLNSRC
CLNACC RCV000157572.1,