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rs267607587

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607587(C;T)
Make rs267607587(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156134901
GeneLMNA
is asnp
is mentioned by
dbSNPrs267607587
ebirs267607587
HLIrs267607587
Exacrs267607587
Varsomers267607587
Maprs267607587
PheGenIrs267607587
hapmaprs267607587
1000 genomesrs267607587
hgdprs267607587
ensemblrs267607587
gopubmedrs267607587
geneviewrs267607587
scholarrs267607587
googlers267607587
pharmgkbrs267607587
gwascentralrs267607587
openSNPrs267607587
23andMers267607587
23andMe allrs267607587
SNP Nexus

SNPshotrs267607587
SNPdbers267607587
MSV3drs267607587
GWAS Ctlgrs267607587
Max Magnitude0
ClinVar
Risk rs267607587(T;T)
Alt rs267607587(T;T)
Reference rs267607587(C;C)
Significance Other
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156104692C>T
CLNSRC
CLNACC RCV000057448.3,