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rs57508089

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs57508089(C;T)
Make rs57508089(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position156136110
GeneLMNA
is asnp
is mentioned by
dbSNPrs57508089
ebirs57508089
HLIrs57508089
Exacrs57508089
Varsomers57508089
Maprs57508089
PheGenIrs57508089
hapmaprs57508089
1000 genomesrs57508089
hgdprs57508089
ensemblrs57508089
gopubmedrs57508089
geneviewrs57508089
scholarrs57508089
googlers57508089
pharmgkbrs57508089
gwascentralrs57508089
openSNPrs57508089
23andMers57508089
23andMe allrs57508089
SNP Nexus

SNPshotrs57508089
SNPdbers57508089
MSV3drs57508089
GWAS Ctlgrs57508089
Max Magnitude0
ClinVar
Risk rs57508089(T;T)
Alt rs57508089(T;T)
Reference rs57508089(C;C)
Significance Pathogenic
Disease Limb-girdle muscular dystrophy not provided
Variation info
Gene LMNA
CLNDBN Limb-girdle muscular dystrophy not provided
Reversed 0
HGVS NC_000001.10:g.156105901C>T
CLNSRC ClinVar Epithelial Biology
CLNACC RCV000041309.3, RCV000057239.2,