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rs267607555

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607555(C;T)
Make rs267607555(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156136009
GeneLMNA
is asnp
is mentioned by
dbSNPrs267607555
ebirs267607555
HLIrs267607555
Exacrs267607555
Varsomers267607555
Maprs267607555
PheGenIrs267607555
hapmaprs267607555
1000 genomesrs267607555
hgdprs267607555
ensemblrs267607555
gopubmedrs267607555
geneviewrs267607555
scholarrs267607555
googlers267607555
pharmgkbrs267607555
gwascentralrs267607555
openSNPrs267607555
23andMers267607555
23andMe allrs267607555
SNP Nexus

SNPshotrs267607555
SNPdbers267607555
MSV3drs267607555
GWAS Ctlgrs267607555
Max Magnitude0
ClinVar
Risk rs267607555(T;T)
Alt rs267607555(T;T)
Reference rs267607555(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156105800C>T
CLNSRC
CLNACC RCV000057218.2,