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rs764243269

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs764243269(A;A)
Make rs764243269(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178587708
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs764243269
ebirs764243269
HLIrs764243269
Exacrs764243269
Varsomers764243269
Maprs764243269
PheGenIrs764243269
hapmaprs764243269
1000 genomesrs764243269
hgdprs764243269
ensemblrs764243269
gopubmedrs764243269
geneviewrs764243269
scholarrs764243269
googlers764243269
pharmgkbrs764243269
gwascentralrs764243269
openSNPrs764243269
23andMers764243269
23andMe allrs764243269
SNP Nexus

SNPshotrs764243269
SNPdbers764243269
MSV3drs764243269
GWAS Ctlgrs764243269
Max Magnitude0
ClinVar
Risk rs764243269(A;A)
Alt rs764243269(A;A)
Reference rs764243269(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000002.11:g.179452435G>A
CLNSRC
CLNACC RCV000209814.1,