rs1057517730
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TGAG;TGAG) | 0 | common in clinvar |
Make rs1057517730(-;-) |
Make rs1057517730(-;AGTG) |
Make rs1057517730(AGTG;AGTG) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | X |
Position | 37796145 |
Gene | CYBB |
is a | snp |
is | mentioned by |
dbSNP | rs1057517730 |
dbSNP (classic) | rs1057517730 |
ClinGen | rs1057517730 |
ebi | rs1057517730 |
HLI | rs1057517730 |
Exac | rs1057517730 |
Gnomad | rs1057517730 |
Varsome | rs1057517730 |
LitVar | rs1057517730 |
Map | rs1057517730 |
PheGenI | rs1057517730 |
Biobank | rs1057517730 |
1000 genomes | rs1057517730 |
hgdp | rs1057517730 |
ensembl | rs1057517730 |
geneview | rs1057517730 |
scholar | rs1057517730 |
rs1057517730 | |
pharmgkb | rs1057517730 |
gwascentral | rs1057517730 |
openSNP | rs1057517730 |
23andMe | rs1057517730 |
SNPshot | rs1057517730 |
SNPdbe | rs1057517730 |
MSV3d | rs1057517730 |
GWAS Ctlg | rs1057517730 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057517730(-;-) |
Alt | rs1057517730(-;-) |
Reference | Rs1057517730(TGAG;TGAG) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | CYBB |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000023.10:g.37655398_37655401delAGTG |
CLNSRC | |
CLNACC | RCV000412938.1, |