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rs267607581

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607581(C;G)
Make rs267607581(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156137651
GeneLMNA
is asnp
is mentioned by
dbSNPrs267607581
ebirs267607581
HLIrs267607581
Exacrs267607581
Varsomers267607581
Maprs267607581
PheGenIrs267607581
hapmaprs267607581
1000 genomesrs267607581
hgdprs267607581
ensemblrs267607581
gopubmedrs267607581
geneviewrs267607581
scholarrs267607581
googlers267607581
pharmgkbrs267607581
gwascentralrs267607581
openSNPrs267607581
23andMers267607581
23andMe allrs267607581
SNP Nexus

SNPshotrs267607581
SNPdbers267607581
MSV3drs267607581
GWAS Ctlgrs267607581
Max Magnitude0
ClinVar
Risk rs267607581(G;G)
Alt rs267607581(G;G)
Reference rs267607581(C;C)
Significance Probable-Pathogenic
Disease not provided Limb-girdle muscular dystrophy
Variation info
Gene LMNA
CLNDBN not provided Limb-girdle muscular dystrophy
Reversed 0
HGVS NC_000001.10:g.156107442C>G
CLNSRC
CLNACC RCV000057338.1, RCV000154514.1,