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rs28928900

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs28928900(C;G)
Make rs28928900(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position156115096
GeneLMNA
is asnp
is mentioned by
dbSNPrs28928900
dbSNP (classic)rs28928900
ClinGenrs28928900
ebirs28928900
HLIrs28928900
Exacrs28928900
Gnomadrs28928900
Varsomers28928900
LitVarrs28928900
Maprs28928900
PheGenIrs28928900
Biobankrs28928900
1000 genomesrs28928900
hgdprs28928900
ensemblrs28928900
geneviewrs28928900
scholarrs28928900
googlers28928900
pharmgkbrs28928900
gwascentralrs28928900
openSNPrs28928900
23andMers28928900
SNPshotrs28928900
SNPdbers28928900
MSV3drs28928900
GWAS Ctlgrs28928900
Max Magnitude0
OMIM150330
DescCARDIOMYOPATHY, DILATED, 1A
Variant0005
Relatedalso



ClinVar
Risk rs28928900(G;G) rs28928900(T;T)
Alt rs28928900(G;G) rs28928900(T;T)
Reference Rs28928900(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 1A Familial partial lipodystrophy 2 not provided not specified
Variation info
Gene LMNA
CLNDBN Dilated cardiomyopathy 1A Familial partial lipodystrophy 2 not provided not specified
Reversed 0
HGVS NC_000001.10:g.156084887C>G; NC_000001.10:g.156084887C>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000015566.25, RCV000015567.25, RCV000057359.1, RCV000156772.1,