rs200910834
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs200910834(C;C) |
Make rs200910834(C;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 10 |
Position | 99727157 |
Gene | COX15 |
is a | snp |
is | mentioned by |
dbSNP | rs200910834 |
dbSNP (classic) | rs200910834 |
ClinGen | rs200910834 |
ebi | rs200910834 |
HLI | rs200910834 |
Exac | rs200910834 |
Gnomad | rs200910834 |
Varsome | rs200910834 |
LitVar | rs200910834 |
Map | rs200910834 |
PheGenI | rs200910834 |
Biobank | rs200910834 |
1000 genomes | rs200910834 |
hgdp | rs200910834 |
ensembl | rs200910834 |
geneview | rs200910834 |
scholar | rs200910834 |
rs200910834 | |
pharmgkb | rs200910834 |
gwascentral | rs200910834 |
openSNP | rs200910834 |
23andMe | rs200910834 |
SNPshot | rs200910834 |
SNPdbe | rs200910834 |
MSV3d | rs200910834 |
GWAS Ctlg | rs200910834 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs200910834(C;C) |
Alt | rs200910834(C;C) |
Reference | Rs200910834(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | COX15 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.101486914G>C |
CLNSRC | |
CLNACC | RCV000266470.1, |