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rs368200299

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs368200299(A;A)
Make rs368200299(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position178620285
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs368200299
ebirs368200299
HLIrs368200299
Exacrs368200299
Varsomers368200299
Maprs368200299
PheGenIrs368200299
hapmaprs368200299
1000 genomesrs368200299
hgdprs368200299
ensemblrs368200299
gopubmedrs368200299
geneviewrs368200299
scholarrs368200299
googlers368200299
pharmgkbrs368200299
gwascentralrs368200299
openSNPrs368200299
23andMers368200299
23andMe allrs368200299
SNP Nexus

SNPshotrs368200299
SNPdbers368200299
MSV3drs368200299
GWAS Ctlgrs368200299
Max Magnitude0
ClinVar
Risk rs368200299(A,T;A,T)
Alt rs368200299(A,T;A,T)
Reference rs368200299(G;G)
Significance Probable-Pathogenic
Disease Dilated cardiomyopathy 1G Familial hypertrophic cardiomyopathy 9 Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Dilated cardiomyopathy 1G Familial hypertrophic cardiomyopathy 9 Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000002.11:g.179485012G>T
CLNSRC
CLNACC RCV000196059.1, RCV000209311.1,