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rs371678190

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs371678190(G;T)
Make rs371678190(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178578066
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs371678190
ebirs371678190
HLIrs371678190
Exacrs371678190
Varsomers371678190
Maprs371678190
PheGenIrs371678190
hapmaprs371678190
1000 genomesrs371678190
hgdprs371678190
ensemblrs371678190
gopubmedrs371678190
geneviewrs371678190
scholarrs371678190
googlers371678190
pharmgkbrs371678190
gwascentralrs371678190
openSNPrs371678190
23andMers371678190
23andMe allrs371678190
SNP Nexus

SNPshotrs371678190
SNPdbers371678190
MSV3drs371678190
GWAS Ctlgrs371678190
Max Magnitude0
ClinVar
Risk rs371678190(A,T;A,T)
Alt rs371678190(A,T;A,T)
Reference rs371678190(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy not provided not specified
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy not provided not specified
Reversed 0
HGVS NC_000002.11:g.179442793G>A; NC_000002.11:g.179442793G>T
CLNSRC
CLNACC RCV000152238.2, RCV000184251.1, RCV000220525.1,