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rs775186117

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs775186117(A;A)
Make rs775186117(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178617393
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs775186117
ebirs775186117
HLIrs775186117
Exacrs775186117
Varsomers775186117
Maprs775186117
PheGenIrs775186117
hapmaprs775186117
1000 genomesrs775186117
hgdprs775186117
ensemblrs775186117
gopubmedrs775186117
geneviewrs775186117
scholarrs775186117
googlers775186117
pharmgkbrs775186117
gwascentralrs775186117
openSNPrs775186117
23andMers775186117
23andMe allrs775186117
SNP Nexus

SNPshotrs775186117
SNPdbers775186117
MSV3drs775186117
GWAS Ctlgrs775186117
Max Magnitude0
ClinVar
Risk rs775186117(A;A)
Alt rs775186117(A;A)
Reference rs775186117(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.179482120G>A
CLNSRC
CLNACC RCV000209289.1,