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rs794726921

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794726921(-;-)
Make rs794726921(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156114966
GeneLMNA
is asnp
is mentioned by
dbSNPrs794726921
ebirs794726921
HLIrs794726921
Exacrs794726921
Varsomers794726921
Maprs794726921
PheGenIrs794726921
hapmaprs794726921
1000 genomesrs794726921
hgdprs794726921
ensemblrs794726921
gopubmedrs794726921
geneviewrs794726921
scholarrs794726921
googlers794726921
pharmgkbrs794726921
gwascentralrs794726921
openSNPrs794726921
23andMers794726921
23andMe allrs794726921
SNP Nexus

SNPshotrs794726921
SNPdbers794726921
MSV3drs794726921
GWAS Ctlgrs794726921
Max Magnitude0
ClinVar
Risk rs794726921(;)
Alt rs794726921(;)
Reference rs794726921(C;C)
Significance Pathogenic
Disease Benign scapuloperoneal muscular dystrophy with cardiomyopathy
Variation info
Gene LMNA
CLNDBN Benign scapuloperoneal muscular dystrophy with cardiomyopathy
Reversed 0
HGVS NC_000001.10:g.156084757delC
CLNSRC
CLNACC RCV000173379.1,