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rs397517888

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397517888(-;-)
Make rs397517888(-;TGGA)
Make rs397517888(TGGA;TGGA)
ReferenceGRCh38 38.1/141
Chromosome1
Position156136079
GeneLMNA
is asnp
is mentioned by
dbSNPrs397517888
ebirs397517888
HLIrs397517888
Exacrs397517888
Varsomers397517888
Maprs397517888
PheGenIrs397517888
hapmaprs397517888
1000 genomesrs397517888
hgdprs397517888
ensemblrs397517888
gopubmedrs397517888
geneviewrs397517888
scholarrs397517888
googlers397517888
pharmgkbrs397517888
gwascentralrs397517888
openSNPrs397517888
23andMers397517888
23andMe allrs397517888
SNP Nexus

SNPshotrs397517888
SNPdbers397517888
MSV3drs397517888
GWAS Ctlgrs397517888
Max Magnitude0
ClinVar
Risk rs397517888(ATGG;ATGG)
Alt rs397517888(ATGG;ATGG)
Reference rs397517888(;)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene LMNA
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000001.10:g.156105867_156105870dupTGGA
CLNSRC ClinVar
CLNACC RCV000041307.2,