rs760743233
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs760743233(C;T) |
Make rs760743233(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 156130726 |
Gene | LMNA |
is a | snp |
is | mentioned by |
dbSNP | rs760743233 |
dbSNP (classic) | rs760743233 |
ClinGen | rs760743233 |
ebi | rs760743233 |
HLI | rs760743233 |
Exac | rs760743233 |
Gnomad | rs760743233 |
Varsome | rs760743233 |
LitVar | rs760743233 |
Map | rs760743233 |
PheGenI | rs760743233 |
Biobank | rs760743233 |
1000 genomes | rs760743233 |
hgdp | rs760743233 |
ensembl | rs760743233 |
geneview | rs760743233 |
scholar | rs760743233 |
rs760743233 | |
pharmgkb | rs760743233 |
gwascentral | rs760743233 |
openSNP | rs760743233 |
23andMe | rs760743233 |
SNPshot | rs760743233 |
SNPdbe | rs760743233 |
MSV3d | rs760743233 |
GWAS Ctlg | rs760743233 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs760743233(T;T) |
Alt | rs760743233(T;T) |
Reference | Rs760743233(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | LMNA |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.156100517C>T |
CLNSRC | |
CLNACC | RCV000182357.1, |