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rs267607590

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607590(A;A)
Make rs267607590(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156136122
GeneLMNA
is asnp
is mentioned by
dbSNPrs267607590
ebirs267607590
HLIrs267607590
Exacrs267607590
Varsomers267607590
Maprs267607590
PheGenIrs267607590
hapmaprs267607590
1000 genomesrs267607590
hgdprs267607590
ensemblrs267607590
gopubmedrs267607590
geneviewrs267607590
scholarrs267607590
googlers267607590
pharmgkbrs267607590
gwascentralrs267607590
openSNPrs267607590
23andMers267607590
23andMe allrs267607590
SNP Nexus

SNPshotrs267607590
SNPdbers267607590
MSV3drs267607590
GWAS Ctlgrs267607590
Max Magnitude0
ClinVar
Risk rs267607590(A;A) rs267607590(T;T)
Alt rs267607590(A;A) rs267607590(T;T)
Reference Rs267607590(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156105913G>A; NC_000001.10:g.156105913G>T
CLNSRC
CLNACC RCV000057242.2, RCV000236305.1,