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rs267607548

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607548(A;A)
Make rs267607548(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156136003
GeneLMNA
is asnp
is mentioned by
dbSNPrs267607548
ebirs267607548
HLIrs267607548
Exacrs267607548
Varsomers267607548
Maprs267607548
PheGenIrs267607548
hapmaprs267607548
1000 genomesrs267607548
hgdprs267607548
ensemblrs267607548
gopubmedrs267607548
geneviewrs267607548
scholarrs267607548
googlers267607548
pharmgkbrs267607548
gwascentralrs267607548
openSNPrs267607548
23andMers267607548
23andMe allrs267607548
SNP Nexus

SNPshotrs267607548
SNPdbers267607548
MSV3drs267607548
GWAS Ctlgrs267607548
Max Magnitude0
ClinVar
Risk rs267607548(A;A)
Alt rs267607548(A;A)
Reference rs267607548(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156105794G>A
CLNSRC
CLNACC RCV000057216.3,