rs794729656
From SNPedia
					| Orientation | minus | 
| Stabilized | minus | 
| Geno | Mag | Summary | 
|---|---|---|
| (T;T) | 0 | common in clinvar | 
| Make rs794729656(A;A) | 
| Make rs794729656(A;T) | 
| Reference | GRCh38.p2 38.2/146 | 
| Chromosome | 3 | 
| Position | 14168389 | 
| Gene | XPC | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs794729656 | 
| dbSNP (classic) | rs794729656 | 
| ClinGen | rs794729656 | 
| ebi | rs794729656 | 
| HLI | rs794729656 | 
| Exac | rs794729656 | 
| Gnomad | rs794729656 | 
| Varsome | rs794729656 | 
| LitVar | rs794729656 | 
| Map | rs794729656 | 
| PheGenI | rs794729656 | 
| Biobank | rs794729656 | 
| 1000 genomes | rs794729656 | 
| hgdp | rs794729656 | 
| ensembl | rs794729656 | 
| geneview | rs794729656 | 
| scholar | rs794729656 | 
| rs794729656 | |
| pharmgkb | rs794729656 | 
| gwascentral | rs794729656 | 
| openSNP | rs794729656 | 
| 23andMe | rs794729656 | 
| SNPshot | rs794729656 | 
| SNPdbe | rs794729656 | 
| MSV3d | rs794729656 | 
| GWAS Ctlg | rs794729656 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs794729656(A;A) | 
| Alt | rs794729656(A;A) | 
| Reference | Rs794729656(T;T) | 
| Significance | Pathogenic | 
| Disease | Xeroderma pigmentosum | 
| Variation | info | 
| Gene | XPC | 
| CLNDBN | Xeroderma pigmentosum, group C | 
| Reversed | 1 | 
| HGVS | NC_000003.11:g.14209889A>T | 
| CLNSRC | OMIM Allelic Variant | 
| CLNACC | RCV000000284.2, | 
