rs745683775
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs745683775(C;G) |
Make rs745683775(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 18 |
Position | 46560448 |
Gene | LOXHD1 |
is a | snp |
is | mentioned by |
dbSNP | rs745683775 |
dbSNP (classic) | rs745683775 |
ClinGen | rs745683775 |
ebi | rs745683775 |
HLI | rs745683775 |
Exac | rs745683775 |
Gnomad | rs745683775 |
Varsome | rs745683775 |
LitVar | rs745683775 |
Map | rs745683775 |
PheGenI | rs745683775 |
Biobank | rs745683775 |
1000 genomes | rs745683775 |
hgdp | rs745683775 |
ensembl | rs745683775 |
geneview | rs745683775 |
scholar | rs745683775 |
rs745683775 | |
pharmgkb | rs745683775 |
gwascentral | rs745683775 |
openSNP | rs745683775 |
23andMe | rs745683775 |
SNPshot | rs745683775 |
SNPdbe | rs745683775 |
MSV3d | rs745683775 |
GWAS Ctlg | rs745683775 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs745683775(G;G) rs745683775(T;T) |
Alt | rs745683775(G;G) rs745683775(T;T) |
Reference | Rs745683775(C;C) |
Significance | Probable-Pathogenic |
Disease | not specified not provided |
Variation | info |
Gene | LOXHD1 |
CLNDBN | not specified not provided |
Reversed | 0 |
HGVS | NC_000018.9:g.44140411C>G |
CLNSRC | |
CLNACC | RCV000219519.1, RCV000485022.1, |