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rs397517902

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397517902(C;C)
Make rs397517902(C;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position156115274
GeneLMNA
is asnp
is mentioned by
dbSNPrs397517902
ebirs397517902
HLIrs397517902
Exacrs397517902
Varsomers397517902
Maprs397517902
PheGenIrs397517902
hapmaprs397517902
1000 genomesrs397517902
hgdprs397517902
ensemblrs397517902
gopubmedrs397517902
geneviewrs397517902
scholarrs397517902
googlers397517902
pharmgkbrs397517902
gwascentralrs397517902
openSNPrs397517902
23andMers397517902
23andMe allrs397517902
SNP Nexus

SNPshotrs397517902
SNPdbers397517902
MSV3drs397517902
GWAS Ctlgrs397517902
Max Magnitude0
ClinVar
Risk rs397517902(C;C)
Alt rs397517902(C;C)
Reference rs397517902(G;G)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene LMNA
CLNDBN not specified not provided
Reversed 0
HGVS NC_000001.10:g.156085065G>C
CLNSRC ClinVar
CLNACC RCV000041347.4, RCV000182394.2,