rs876657650
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs876657650(-;-) |
Make rs876657650(-;A) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 1 |
Position | 156130736 |
Gene | LMNA |
is a | snp |
is | mentioned by |
dbSNP | rs876657650 |
dbSNP (classic) | rs876657650 |
ClinGen | rs876657650 |
ebi | rs876657650 |
HLI | rs876657650 |
Exac | rs876657650 |
Gnomad | rs876657650 |
Varsome | rs876657650 |
LitVar | rs876657650 |
Map | rs876657650 |
PheGenI | rs876657650 |
Biobank | rs876657650 |
1000 genomes | rs876657650 |
hgdp | rs876657650 |
ensembl | rs876657650 |
geneview | rs876657650 |
scholar | rs876657650 |
rs876657650 | |
pharmgkb | rs876657650 |
gwascentral | rs876657650 |
openSNP | rs876657650 |
23andMe | rs876657650 |
SNPshot | rs876657650 |
SNPdbe | rs876657650 |
MSV3d | rs876657650 |
GWAS Ctlg | rs876657650 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876657650(-;-) |
Alt | rs876657650(-;-) |
Reference | Rs876657650(A;A) |
Significance | Probable-Pathogenic |
Disease | Primary dilated cardiomyopathy |
Variation | info |
Gene | LMNA |
CLNDBN | Primary dilated cardiomyopathy |
Reversed | 0 |
HGVS | NC_000001.10:g.156100527delA |
CLNSRC | |
CLNACC | RCV000223332.1, |