rs878853030
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs878853030(-;-) |
Make rs878853030(-;C) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | X |
Position | 108692768 |
Gene | COL4A5 |
is a | snp |
is | mentioned by |
dbSNP | rs878853030 |
dbSNP (classic) | rs878853030 |
ClinGen | rs878853030 |
ebi | rs878853030 |
HLI | rs878853030 |
Exac | rs878853030 |
Gnomad | rs878853030 |
Varsome | rs878853030 |
LitVar | rs878853030 |
Map | rs878853030 |
PheGenI | rs878853030 |
Biobank | rs878853030 |
1000 genomes | rs878853030 |
hgdp | rs878853030 |
ensembl | rs878853030 |
geneview | rs878853030 |
scholar | rs878853030 |
rs878853030 | |
pharmgkb | rs878853030 |
gwascentral | rs878853030 |
openSNP | rs878853030 |
23andMe | rs878853030 |
SNPshot | rs878853030 |
SNPdbe | rs878853030 |
MSV3d | rs878853030 |
GWAS Ctlg | rs878853030 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs878853030(-;-) |
Alt | rs878853030(-;-) |
Reference | Rs878853030(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | COL4A5 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000023.10:g.107935998delC |
CLNSRC | |
CLNACC | RCV000224452.1, |