rs267607545
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs267607545(A;A) |
Make rs267607545(A;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 1 |
Position | 156136121 |
Gene | LMNA |
is a | snp |
is | mentioned by |
dbSNP | rs267607545 |
dbSNP (classic) | rs267607545 |
ClinGen | rs267607545 |
ebi | rs267607545 |
HLI | rs267607545 |
Exac | rs267607545 |
Gnomad | rs267607545 |
Varsome | rs267607545 |
LitVar | rs267607545 |
Map | rs267607545 |
PheGenI | rs267607545 |
Biobank | rs267607545 |
1000 genomes | rs267607545 |
hgdp | rs267607545 |
ensembl | rs267607545 |
geneview | rs267607545 |
scholar | rs267607545 |
rs267607545 | |
pharmgkb | rs267607545 |
gwascentral | rs267607545 |
openSNP | rs267607545 |
23andMe | rs267607545 |
SNPshot | rs267607545 |
SNPdbe | rs267607545 |
MSV3d | rs267607545 |
GWAS Ctlg | rs267607545 |
Max Magnitude | 0 |
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, |