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rs878853220

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878853220(G;G)
Make rs878853220(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position156130818
GeneLMNA
is asnp
is mentioned by
dbSNPrs878853220
ebirs878853220
HLIrs878853220
Exacrs878853220
Varsomers878853220
Maprs878853220
PheGenIrs878853220
hapmaprs878853220
1000 genomesrs878853220
hgdprs878853220
ensemblrs878853220
gopubmedrs878853220
geneviewrs878853220
scholarrs878853220
googlers878853220
pharmgkbrs878853220
gwascentralrs878853220
openSNPrs878853220
23andMers878853220
23andMe allrs878853220
SNP Nexus

SNPshotrs878853220
SNPdbers878853220
MSV3drs878853220
GWAS Ctlgrs878853220
Max Magnitude0
ClinVar
Risk rs878853220(G;G)
Alt rs878853220(G;G)
Reference rs878853220(T;T)
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.156100609T>G
CLNSRC
CLNACC RCV000225043.1,