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rs730882262

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730882262(G;G)
Make rs730882262(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156135293
GeneLMNA
is asnp
is mentioned by
dbSNPrs730882262
ebirs730882262
HLIrs730882262
Exacrs730882262
Varsomers730882262
Maprs730882262
PheGenIrs730882262
hapmaprs730882262
1000 genomesrs730882262
hgdprs730882262
ensemblrs730882262
gopubmedrs730882262
geneviewrs730882262
scholarrs730882262
googlers730882262
pharmgkbrs730882262
gwascentralrs730882262
openSNPrs730882262
23andMers730882262
23andMe allrs730882262
SNP Nexus

SNPshotrs730882262
SNPdbers730882262
MSV3drs730882262
GWAS Ctlgrs730882262
Max Magnitude0
ClinVar
Risk rs730882262(C,G;C,G)
Alt rs730882262(C,G;C,G)
Reference rs730882262(T;T)
Significance Pathogenic
Disease not provided Hutchinson-Gilford progeria syndrome Right ventricular cardiomyopathy
Variation info
Gene LMNA
CLNDBN not provided Hutchinson-Gilford progeria syndrome, childhood-onset Right ventricular cardiomyopathy
Reversed 0
HGVS NC_000001.10:g.156105084T>C; NC_000001.10:g.156105084T>G
CLNSRC
CLNACC RCV000235583.1, RCV000162192.1,