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rs727504799

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504799(C;C)
Make rs727504799(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178609683
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs727504799
ebirs727504799
HLIrs727504799
Exacrs727504799
Varsomers727504799
Maprs727504799
PheGenIrs727504799
hapmaprs727504799
1000 genomesrs727504799
hgdprs727504799
ensemblrs727504799
gopubmedrs727504799
geneviewrs727504799
scholarrs727504799
googlers727504799
pharmgkbrs727504799
gwascentralrs727504799
openSNPrs727504799
23andMers727504799
23andMe allrs727504799
SNP Nexus

SNPshotrs727504799
SNPdbers727504799
MSV3drs727504799
GWAS Ctlgrs727504799
Max Magnitude0
ClinVar
Risk rs727504799(C;C)
Alt rs727504799(C;C)
Reference rs727504799(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179474410C>G
CLNSRC
CLNACC RCV000156125.1,