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rs281864908

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281864908(A;A)
Make rs281864908(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position178738108
GeneTTN
is asnp
is mentioned by
dbSNPrs281864908
ebirs281864908
HLIrs281864908
Exacrs281864908
Varsomers281864908
Maprs281864908
PheGenIrs281864908
hapmaprs281864908
1000 genomesrs281864908
hgdprs281864908
ensemblrs281864908
gopubmedrs281864908
geneviewrs281864908
scholarrs281864908
googlers281864908
pharmgkbrs281864908
gwascentralrs281864908
openSNPrs281864908
23andMers281864908
23andMe allrs281864908
SNP Nexus

SNPshotrs281864908
SNPdbers281864908
MSV3drs281864908
GWAS Ctlgrs281864908
Max Magnitude0
ClinVar
Risk rs281864908(A;A)
Alt rs281864908(A;A)
Reference rs281864908(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 1G
Variation info
Gene
CLNDBN Dilated cardiomyopathy 1G
Reversed 1
HGVS NC_000002.11:g.179602835C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013494.1,