Have questions? Visit https://www.reddit.com/r/SNPedia

rs267607545

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607545(A;A)
Make rs267607545(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position156136121
GeneLMNA
is asnp
is mentioned by
dbSNPrs267607545
dbSNP (classic)rs267607545
ClinGenrs267607545
ebirs267607545
HLIrs267607545
Exacrs267607545
Gnomadrs267607545
Varsomers267607545
LitVarrs267607545
Maprs267607545
PheGenIrs267607545
Biobankrs267607545
1000 genomesrs267607545
hgdprs267607545
ensemblrs267607545
geneviewrs267607545
scholarrs267607545
googlers267607545
pharmgkbrs267607545
gwascentralrs267607545
openSNPrs267607545
23andMers267607545
23andMe allrs267607545
SNPshotrs267607545
SNPdbers267607545
MSV3drs267607545
GWAS Ctlgrs267607545
Max Magnitude0
ClinVar
Risk rs267607545(A;A) rs267607545(C;C) rs267607545(T;T)
Alt rs267607545(A;A) rs267607545(C;C) rs267607545(T;T)
Reference Rs267607545(G;G)
Significance Pathogenic
Disease not provided Cardiovascular phenotype
Variation info
Gene LMNA
CLNDBN not provided Cardiovascular phenotype
Reversed 0
HGVS NC_000001.10:g.156105912G>A; NC_000001.10:g.156105912G>C; NC_000001.10:g.156105912G>T
CLNSRC UniProtKB (protein)
CLNACC RCV000057243.1, RCV000248263.1, RCV000057244.1,