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rs267607540

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGA;AGA) 0 common in clinvar
Make rs267607540(-;-)
Make rs267607540(-;AAG)
Make rs267607540(AAG;AAG)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156134511
GeneLMNA
is asnp
is mentioned by
dbSNPrs267607540
ClinGenrs267607540
ebirs267607540
HLIrs267607540
Exacrs267607540
Varsomers267607540
Maprs267607540
PheGenIrs267607540
hapmaprs267607540
1000 genomesrs267607540
hgdprs267607540
ensemblrs267607540
gopubmedrs267607540
geneviewrs267607540
scholarrs267607540
googlers267607540
pharmgkbrs267607540
gwascentralrs267607540
openSNPrs267607540
23andMers267607540
23andMe allrs267607540
SNP Nexus

SNPshotrs267607540
SNPdbers267607540
MSV3drs267607540
GWAS Ctlgrs267607540
Merged fromRs267607551
Max Magnitude0
ClinVar
Risk rs267607540(-;-) rs267607540(GAA;GAA)
Alt rs267607540(-;-) rs267607540(GAA;GAA)
Reference rs267607540(AAG;AAG)
Significance Pathogenic
Disease Limb-girdle muscular dystrophy not provided
Variation info
Gene LMNA
CLNDBN Limb-girdle muscular dystrophy, type 1B not provided
Reversed 0
HGVS NC_000001.10:g.156104304_156104306delGAA
CLNSRC OMIM Allelic Variant
CLNACC RCV000015588.26, RCV000057433.2,