rs749272546
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs749272546(-;-) |
Make rs749272546(-;C) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 6 |
Position | 69701470 |
Gene | LMBRD1 |
is a | snp |
is | mentioned by |
dbSNP | rs749272546 |
dbSNP (classic) | rs749272546 |
ClinGen | rs749272546 |
ebi | rs749272546 |
HLI | rs749272546 |
Exac | rs749272546 |
Gnomad | rs749272546 |
Varsome | rs749272546 |
LitVar | rs749272546 |
Map | rs749272546 |
PheGenI | rs749272546 |
Biobank | rs749272546 |
1000 genomes | rs749272546 |
hgdp | rs749272546 |
ensembl | rs749272546 |
geneview | rs749272546 |
scholar | rs749272546 |
rs749272546 | |
pharmgkb | rs749272546 |
gwascentral | rs749272546 |
openSNP | rs749272546 |
23andMe | rs749272546 |
SNPshot | rs749272546 |
SNPdbe | rs749272546 |
MSV3d | rs749272546 |
GWAS Ctlg | rs749272546 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs749272546(-;-) |
Alt | rs749272546(-;-) |
Reference | Rs749272546(C;C) |
Significance | Pathogenic |
Disease | Inborn genetic diseases not provided |
Variation | info |
Gene | LMBRD1 |
CLNDBN | Inborn genetic diseases not provided |
Reversed | 0 |
HGVS | NC_000006.11:g.70411362delC |
CLNSRC | |
CLNACC | RCV000210618.1, RCV000255705.1, |