rs1057517778
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs1057517778(-;-) |
Make rs1057517778(-;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | X |
Position | 30308784 |
Gene | NR0B1 |
is a | snp |
is | mentioned by |
dbSNP | rs1057517778 |
dbSNP (classic) | rs1057517778 |
ClinGen | rs1057517778 |
ebi | rs1057517778 |
HLI | rs1057517778 |
Exac | rs1057517778 |
Gnomad | rs1057517778 |
Varsome | rs1057517778 |
LitVar | rs1057517778 |
Map | rs1057517778 |
PheGenI | rs1057517778 |
Biobank | rs1057517778 |
1000 genomes | rs1057517778 |
hgdp | rs1057517778 |
ensembl | rs1057517778 |
geneview | rs1057517778 |
scholar | rs1057517778 |
rs1057517778 | |
pharmgkb | rs1057517778 |
gwascentral | rs1057517778 |
openSNP | rs1057517778 |
23andMe | rs1057517778 |
SNPshot | rs1057517778 |
SNPdbe | rs1057517778 |
MSV3d | rs1057517778 |
GWAS Ctlg | rs1057517778 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057517778(-;-) |
Alt | rs1057517778(-;-) |
Reference | Rs1057517778(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | NR0B1 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000023.10:g.30326901delC |
CLNSRC | |
CLNACC | RCV000413027.1, |