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rs760743233

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs760743233(C;T)
Make rs760743233(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156130726
GeneLMNA
is asnp
is mentioned by
dbSNPrs760743233
ebirs760743233
HLIrs760743233
Exacrs760743233
Varsomers760743233
Maprs760743233
PheGenIrs760743233
hapmaprs760743233
1000 genomesrs760743233
hgdprs760743233
ensemblrs760743233
gopubmedrs760743233
geneviewrs760743233
scholarrs760743233
googlers760743233
pharmgkbrs760743233
gwascentralrs760743233
openSNPrs760743233
23andMers760743233
23andMe allrs760743233
SNP Nexus

SNPshotrs760743233
SNPdbers760743233
MSV3drs760743233
GWAS Ctlgrs760743233
Max Magnitude0
ClinVar
Risk rs760743233(T;T)
Alt rs760743233(T;T)
Reference rs760743233(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156100517C>T
CLNSRC
CLNACC RCV000182357.1,