rs869025275
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs869025275(A;A) |
Make rs869025275(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 3 |
Position | 14152417 |
Gene | XPC |
is a | snp |
is | mentioned by |
dbSNP | rs869025275 |
dbSNP (classic) | rs869025275 |
ClinGen | rs869025275 |
ebi | rs869025275 |
HLI | rs869025275 |
Exac | rs869025275 |
Gnomad | rs869025275 |
Varsome | rs869025275 |
LitVar | rs869025275 |
Map | rs869025275 |
PheGenI | rs869025275 |
Biobank | rs869025275 |
1000 genomes | rs869025275 |
hgdp | rs869025275 |
ensembl | rs869025275 |
geneview | rs869025275 |
scholar | rs869025275 |
rs869025275 | |
pharmgkb | rs869025275 |
gwascentral | rs869025275 |
openSNP | rs869025275 |
23andMe | rs869025275 |
SNPshot | rs869025275 |
SNPdbe | rs869025275 |
MSV3d | rs869025275 |
GWAS Ctlg | rs869025275 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs869025275(A;A) |
Alt | rs869025275(A;A) |
Reference | Rs869025275(G;G) |
Significance | Probable-Pathogenic |
Disease | Xeroderma pigmentosum |
Variation | info |
Gene | XPC |
CLNDBN | Xeroderma pigmentosum, type 1 |
Reversed | 1 |
HGVS | NC_000003.11:g.14193917C>T |
CLNSRC | |
CLNACC | RCV000207299.1, |