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rs777602537

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs777602537(A;A)
Make rs777602537(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178576614
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs777602537
ebirs777602537
HLIrs777602537
Exacrs777602537
Varsomers777602537
Maprs777602537
PheGenIrs777602537
hapmaprs777602537
1000 genomesrs777602537
hgdprs777602537
ensemblrs777602537
gopubmedrs777602537
geneviewrs777602537
scholarrs777602537
googlers777602537
pharmgkbrs777602537
gwascentralrs777602537
openSNPrs777602537
23andMers777602537
23andMe allrs777602537
SNP Nexus

SNPshotrs777602537
SNPdbers777602537
MSV3drs777602537
GWAS Ctlgrs777602537
Max Magnitude0
ClinVar
Risk rs777602537(A;A)
Alt rs777602537(A;A)
Reference rs777602537(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.179441341G>T
CLNSRC
CLNACC RCV000208894.1,