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rs267607572

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607572(G;G)
Make rs267607572(G;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position156134518
GeneLMNA
is asnp
is mentioned by
dbSNPrs267607572
ebirs267607572
HLIrs267607572
Exacrs267607572
Varsomers267607572
Maprs267607572
PheGenIrs267607572
hapmaprs267607572
1000 genomesrs267607572
hgdprs267607572
ensemblrs267607572
gopubmedrs267607572
geneviewrs267607572
scholarrs267607572
googlers267607572
pharmgkbrs267607572
gwascentralrs267607572
openSNPrs267607572
23andMers267607572
23andMe allrs267607572
SNP Nexus

SNPshotrs267607572
SNPdbers267607572
MSV3drs267607572
GWAS Ctlgrs267607572
Max Magnitude0
ClinVar
Risk rs267607572(G;G)
Alt rs267607572(G;G)
Reference rs267607572(T;T)
Significance Untested
Disease not specified not provided
Variation info
Gene LMNA
CLNDBN not specified not provided
Reversed 0
HGVS NC_000001.10:g.156104309T>G
CLNSRC ClinVar Epithelial Biology
CLNACC RCV000041357.2, RCV000057435.1,