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rs876657650

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876657650(-;-)
Make rs876657650(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position156130736
GeneLMNA
is asnp
is mentioned by
dbSNPrs876657650
ebirs876657650
HLIrs876657650
Exacrs876657650
Varsomers876657650
Maprs876657650
PheGenIrs876657650
hapmaprs876657650
1000 genomesrs876657650
hgdprs876657650
ensemblrs876657650
gopubmedrs876657650
geneviewrs876657650
scholarrs876657650
googlers876657650
pharmgkbrs876657650
gwascentralrs876657650
openSNPrs876657650
23andMers876657650
23andMe allrs876657650
SNP Nexus

SNPshotrs876657650
SNPdbers876657650
MSV3drs876657650
GWAS Ctlgrs876657650
Max Magnitude0
ClinVar
Risk rs876657650(;)
Alt rs876657650(;)
Reference rs876657650(A;A)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene LMNA
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000001.10:g.156100527delA
CLNSRC
CLNACC RCV000223332.1,