rs676785
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs676785(A;A) |
| Make rs676785(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 25408711 |
| Gene | RHCE |
| is a | snp |
| is | mentioned by |
| dbSNP | rs676785 |
| dbSNP (classic) | rs676785 |
| ClinGen | rs676785 |
| ebi | rs676785 |
| HLI | rs676785 |
| Exac | rs676785 |
| Gnomad | rs676785 |
| Varsome | rs676785 |
| LitVar | rs676785 |
| Map | rs676785 |
| PheGenI | rs676785 |
| Biobank | rs676785 |
| 1000 genomes | rs676785 |
| hgdp | rs676785 |
| ensembl | rs676785 |
| geneview | rs676785 |
| scholar | rs676785 |
| rs676785 | |
| pharmgkb | rs676785 |
| gwascentral | rs676785 |
| openSNP | rs676785 |
| 23andMe | rs676785 |
| SNPshot | rs676785 |
| SNPdbe | rs676785 |
| MSV3d | rs676785 |
| GWAS Ctlg | rs676785 |
| GMAF | 0.1221 |
| Max Magnitude | 0 |
Rh C/c blood group
[PMID 21257350
] DNA-based methods in the immunohematology reference laboratory.
| ClinVar | |
|---|---|
| Risk | rs676785(A;A) |
| Alt | rs676785(A;A) |
| Reference | Rs676785(G;G) |
| Significance | Non-pathogenic |
| Disease | RH C/c POLYMORPHISM not provided |
| Variation | info |
| Gene | RHCE |
| CLNDBN | RH C/c POLYMORPHISM not provided |
| Reversed | 0 |
| HGVS | NC_000001.10:g.25735202G\x3d; NC_000001.10:g.25735202G>A |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000019283.2, RCV000144442.1, |
