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rs121908339

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121908339(A;T)
Make rs121908339(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position86687107
GeneLDB3
is asnp
is mentioned by
dbSNPrs121908339
ebirs121908339
HLIrs121908339
Exacrs121908339
Varsomers121908339
Maprs121908339
PheGenIrs121908339
hapmaprs121908339
1000 genomesrs121908339
hgdprs121908339
ensemblrs121908339
gopubmedrs121908339
geneviewrs121908339
scholarrs121908339
googlers121908339
pharmgkbrs121908339
gwascentralrs121908339
openSNPrs121908339
23andMers121908339
23andMe allrs121908339
SNP Nexus

SNPshotrs121908339
SNPdbers121908339
MSV3drs121908339
GWAS Ctlgrs121908339
Max Magnitude0
OMIM605906
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121908339(T;T)
Alt rs121908339(T;T)
Reference rs121908339(A;A)
Significance Pathogenic
Disease Dilated cardiomyopathy 1C
Variation info
Gene LDB3
CLNDBN Dilated cardiomyopathy 1C
Reversed 0
HGVS NC_000010.10:g.88446864A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000004999.3,