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rs59270054

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs59270054(A;A)
Make rs59270054(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156115162
GeneLMNA
is asnp
is mentioned by
dbSNPrs59270054
ebirs59270054
HLIrs59270054
Exacrs59270054
Varsomers59270054
Maprs59270054
PheGenIrs59270054
hapmaprs59270054
1000 genomesrs59270054
hgdprs59270054
ensemblrs59270054
gopubmedrs59270054
geneviewrs59270054
scholarrs59270054
googlers59270054
pharmgkbrs59270054
gwascentralrs59270054
openSNPrs59270054
23andMers59270054
23andMe allrs59270054
SNP Nexus

SNPshotrs59270054
SNPdbers59270054
MSV3drs59270054
GWAS Ctlgrs59270054
Max Magnitude0
ClinVar
Risk rs59270054(A;A)
Alt rs59270054(A;A)
Reference rs59270054(G;G)
Significance Pathogenic
Disease not provided Primary dilated cardiomyopathy
Variation info
Gene LMNA
CLNDBN not provided Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000001.10:g.156084953G>A
CLNSRC
CLNACC RCV000057380.1, RCV000156060.1,