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rs28928903

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs28928903(C;C)
Make rs28928903(C;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position156115087
GeneLMNA
is asnp
is mentioned by
dbSNPrs28928903
ebirs28928903
HLIrs28928903
Exacrs28928903
Varsomers28928903
Maprs28928903
PheGenIrs28928903
hapmaprs28928903
1000 genomesrs28928903
hgdprs28928903
ensemblrs28928903
gopubmedrs28928903
geneviewrs28928903
scholarrs28928903
googlers28928903
pharmgkbrs28928903
gwascentralrs28928903
openSNPrs28928903
23andMers28928903
23andMe allrs28928903
SNP Nexus

SNPshotrs28928903
SNPdbers28928903
MSV3drs28928903
GWAS Ctlgrs28928903
Max Magnitude0
OMIM150330
DescWERNER SYNDROME, ATYPICAL
Variant0030
Relatedalso
Neighborrs28928900
Distance9


ClinVar
Risk rs28928903(C;C)
Alt rs28928903(C;C)
Reference rs28928903(G;G)
Significance Pathogenic
Disease Cardiomyopathy not provided
Variation info
Gene LMNA
CLNDBN Cardiomyopathy, dilated, with hypergonadotripic hypogonadism not provided
Reversed 0
HGVS NC_000001.10:g.156084878G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000015600.23, RCV000057349.1,