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rs59332535

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs59332535(A;A)
Make rs59332535(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156134911
GeneLMNA
is asnp
is mentioned by
dbSNPrs59332535
ebirs59332535
HLIrs59332535
Exacrs59332535
Varsomers59332535
Maprs59332535
PheGenIrs59332535
hapmaprs59332535
1000 genomesrs59332535
hgdprs59332535
ensemblrs59332535
gopubmedrs59332535
geneviewrs59332535
scholarrs59332535
googlers59332535
pharmgkbrs59332535
gwascentralrs59332535
openSNPrs59332535
23andMers59332535
23andMe allrs59332535
SNP Nexus

SNPshotrs59332535
SNPdbers59332535
MSV3drs59332535
GWAS Ctlgrs59332535
Max Magnitude0
ClinVar
Risk rs59332535(A;A)
Alt rs59332535(A;A)
Reference rs59332535(G;G)
Significance Pathogenic
Disease not provided Benign scapuloperoneal muscular dystrophy with cardiomyopathy
Variation info
Gene LMNA
CLNDBN not provided Benign scapuloperoneal muscular dystrophy with cardiomyopathy
Reversed 0
HGVS NC_000001.10:g.156104702G>A
CLNSRC Quest Diagnostics
CLNACC RCV000057453.1, RCV000201012.1,