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rs267607552

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607552(A;A)
Make rs267607552(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156136437
GeneLMNA
is asnp
is mentioned by
dbSNPrs267607552
ebirs267607552
HLIrs267607552
Exacrs267607552
Varsomers267607552
Maprs267607552
PheGenIrs267607552
hapmaprs267607552
1000 genomesrs267607552
hgdprs267607552
ensemblrs267607552
gopubmedrs267607552
geneviewrs267607552
scholarrs267607552
googlers267607552
pharmgkbrs267607552
gwascentralrs267607552
openSNPrs267607552
23andMers267607552
23andMe allrs267607552
SNP Nexus

SNPshotrs267607552
SNPdbers267607552
MSV3drs267607552
GWAS Ctlgrs267607552
Max Magnitude0
ClinVar
Risk rs267607552(A;A)
Alt rs267607552(A;A)
Reference rs267607552(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156106228G>A
CLNSRC
CLNACC RCV000057283.3,