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rs869025458

From SNPedia

Orientationplus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs869025458(AG;AG)
Make rs869025458(AG;GC)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position156115272
GeneLMNA
is asnp
is mentioned by
dbSNPrs869025458
ebirs869025458
HLIrs869025458
Exacrs869025458
Varsomers869025458
Maprs869025458
PheGenIrs869025458
hapmaprs869025458
1000 genomesrs869025458
hgdprs869025458
ensemblrs869025458
gopubmedrs869025458
geneviewrs869025458
scholarrs869025458
googlers869025458
pharmgkbrs869025458
gwascentralrs869025458
openSNPrs869025458
23andMers869025458
23andMe allrs869025458
SNP Nexus

SNPshotrs869025458
SNPdbers869025458
MSV3drs869025458
GWAS Ctlgrs869025458
Max Magnitude0
ClinVar
Risk rs869025458(AG;AG)
Alt rs869025458(AG;AG)
Reference rs869025458(GC;GC)
Significance Probable-Pathogenic
Disease Cardiac conduction defect
Variation info
Gene LMNA
CLNDBN Cardiac conduction defect, nonspecific
Reversed 0
HGVS NC_000001.10:g.156085063_156085064delGCinsAG
CLNSRC
CLNACC RCV000208251.1,