rs201663231
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs201663231(C;G) |
Make rs201663231(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 10 |
Position | 99714620 |
Gene | COX15 |
is a | snp |
is | mentioned by |
dbSNP | rs201663231 |
dbSNP (classic) | rs201663231 |
ClinGen | rs201663231 |
ebi | rs201663231 |
HLI | rs201663231 |
Exac | rs201663231 |
Gnomad | rs201663231 |
Varsome | rs201663231 |
LitVar | rs201663231 |
Map | rs201663231 |
PheGenI | rs201663231 |
Biobank | rs201663231 |
1000 genomes | rs201663231 |
hgdp | rs201663231 |
ensembl | rs201663231 |
geneview | rs201663231 |
scholar | rs201663231 |
rs201663231 | |
pharmgkb | rs201663231 |
gwascentral | rs201663231 |
openSNP | rs201663231 |
23andMe | rs201663231 |
SNPshot | rs201663231 |
SNPdbe | rs201663231 |
MSV3d | rs201663231 |
GWAS Ctlg | rs201663231 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs201663231(G;G) |
Alt | rs201663231(G;G) |
Reference | Rs201663231(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | COX15 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.101474377C>G |
CLNSRC | |
CLNACC | RCV000195737.2, |