rs768324201
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs768324201(A;A) |
| Make rs768324201(A;G) |
| Make rs768324201(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 6 |
| Position | 79060680 |
| Gene | PHIP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs768324201 |
| dbSNP (classic) | rs768324201 |
| ClinGen | rs768324201 |
| ebi | rs768324201 |
| HLI | rs768324201 |
| Exac | rs768324201 |
| Gnomad | rs768324201 |
| Varsome | rs768324201 |
| LitVar | rs768324201 |
| Map | rs768324201 |
| PheGenI | rs768324201 |
| Biobank | rs768324201 |
| 1000 genomes | rs768324201 |
| hgdp | rs768324201 |
| ensembl | rs768324201 |
| geneview | rs768324201 |
| scholar | rs768324201 |
| rs768324201 | |
| pharmgkb | rs768324201 |
| gwascentral | rs768324201 |
| openSNP | rs768324201 |
| 23andMe | rs768324201 |
| SNPshot | rs768324201 |
| SNPdbe | rs768324201 |
| MSV3d | rs768324201 |
| GWAS Ctlg | rs768324201 |
| Max Magnitude | 0 |
aka NM_017934.6(PHIP):c.328C>A or (p.Arg110Ser)
OMIM pathogenic variant
