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rs267607629

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607629(C;G)
Make rs267607629(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156134507
GeneLMNA
is asnp
is mentioned by
dbSNPrs267607629
ebirs267607629
HLIrs267607629
Exacrs267607629
Varsomers267607629
Maprs267607629
PheGenIrs267607629
hapmaprs267607629
1000 genomesrs267607629
hgdprs267607629
ensemblrs267607629
gopubmedrs267607629
geneviewrs267607629
scholarrs267607629
googlers267607629
pharmgkbrs267607629
gwascentralrs267607629
openSNPrs267607629
23andMers267607629
23andMe allrs267607629
SNP Nexus

SNPshotrs267607629
SNPdbers267607629
MSV3drs267607629
GWAS Ctlgrs267607629
Max Magnitude0
ClinVar
Risk rs267607629(G;G)
Alt rs267607629(G;G)
Reference rs267607629(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156104298C>G
CLNSRC
CLNACC RCV000057431.3,