rs7959052
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs7959052(C;C) |
| Make rs7959052(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 52811973 |
| Gene | KRT4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7959052 |
| dbSNP (classic) | rs7959052 |
| ClinGen | rs7959052 |
| ebi | rs7959052 |
| HLI | rs7959052 |
| Exac | rs7959052 |
| Gnomad | rs7959052 |
| Varsome | rs7959052 |
| LitVar | rs7959052 |
| Map | rs7959052 |
| PheGenI | rs7959052 |
| Biobank | rs7959052 |
| 1000 genomes | rs7959052 |
| hgdp | rs7959052 |
| ensembl | rs7959052 |
| geneview | rs7959052 |
| scholar | rs7959052 |
| rs7959052 | |
| pharmgkb | rs7959052 |
| gwascentral | rs7959052 |
| openSNP | rs7959052 |
| 23andMe | rs7959052 |
| SNPshot | rs7959052 |
| SNPdbe | rs7959052 |
| MSV3d | rs7959052 |
| GWAS Ctlg | rs7959052 |
| GMAF | 0.2328 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| ClinVar | |
|---|---|
| Risk | rs7959052(C;C) |
| Alt | rs7959052(C;C) |
| Reference | Rs7959052(T;T) |
| Significance | Non-pathogenic |
| Disease | White sponge nevus of cannon |
| Variation | info |
| Gene | KRT4 |
| CLNDBN | White sponge nevus of cannon |
| Reversed | 0 |
| HGVS | NC_000012.11:g.53205757T>C |
| CLNSRC | |
| CLNACC | RCV000351655.1, |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 12
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Affy500k
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
