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rs267607563

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607563(A;A)
Make rs267607563(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156136252
GeneLMNA
is asnp
is mentioned by
dbSNPrs267607563
ebirs267607563
HLIrs267607563
Exacrs267607563
Varsomers267607563
Maprs267607563
PheGenIrs267607563
hapmaprs267607563
1000 genomesrs267607563
hgdprs267607563
ensemblrs267607563
gopubmedrs267607563
geneviewrs267607563
scholarrs267607563
googlers267607563
pharmgkbrs267607563
gwascentralrs267607563
openSNPrs267607563
23andMers267607563
23andMe allrs267607563
SNP Nexus

SNPshotrs267607563
SNPdbers267607563
MSV3drs267607563
GWAS Ctlgrs267607563
Max Magnitude0
ClinVar
Risk rs267607563(A;A)
Alt rs267607563(A;A)
Reference rs267607563(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156106043G>A
CLNSRC
CLNACC RCV000057256.2,