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rs267607571

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607571(A;A)
Make rs267607571(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156134458
GeneLMNA
is asnp
is mentioned by
dbSNPrs267607571
ebirs267607571
HLIrs267607571
Exacrs267607571
Varsomers267607571
Maprs267607571
PheGenIrs267607571
hapmaprs267607571
1000 genomesrs267607571
hgdprs267607571
ensemblrs267607571
gopubmedrs267607571
geneviewrs267607571
scholarrs267607571
googlers267607571
pharmgkbrs267607571
gwascentralrs267607571
openSNPrs267607571
23andMers267607571
23andMe allrs267607571
SNP Nexus

SNPshotrs267607571
SNPdbers267607571
MSV3drs267607571
GWAS Ctlgrs267607571
Max Magnitude0
ClinVar
Risk rs267607571(A;A)
Alt rs267607571(A;A)
Reference rs267607571(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156104249G>A
CLNSRC
CLNACC RCV000057421.2,