rs747523570
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs747523570(A;A) |
Make rs747523570(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 10 |
Position | 86718086 |
Gene | LDB3 |
is a | snp |
is | mentioned by |
dbSNP | rs747523570 |
dbSNP (classic) | rs747523570 |
ClinGen | rs747523570 |
ebi | rs747523570 |
HLI | rs747523570 |
Exac | rs747523570 |
Gnomad | rs747523570 |
Varsome | rs747523570 |
LitVar | rs747523570 |
Map | rs747523570 |
PheGenI | rs747523570 |
Biobank | rs747523570 |
1000 genomes | rs747523570 |
hgdp | rs747523570 |
ensembl | rs747523570 |
geneview | rs747523570 |
scholar | rs747523570 |
rs747523570 | |
pharmgkb | rs747523570 |
gwascentral | rs747523570 |
openSNP | rs747523570 |
23andMe | rs747523570 |
SNPshot | rs747523570 |
SNPdbe | rs747523570 |
MSV3d | rs747523570 |
GWAS Ctlg | rs747523570 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs747523570(A;A) rs747523570(C;C) |
Alt | rs747523570(A;A) rs747523570(C;C) |
Reference | Rs747523570(G;G) |
Significance | Probable-Pathogenic |
Disease | not specified not provided |
Variation | info |
Gene | LDB3 |
CLNDBN | not specified not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.88477843G>A; NC_000010.10:g.88477843G>C |
CLNSRC | |
CLNACC | RCV000183541.2, RCV000171181.1, |