rs1369766
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1369766(A;A) |
| Make rs1369766(A;G) |
| Make rs1369766(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 18 |
| Position | 51492510 |
| Gene | LINC01630 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1369766 |
| dbSNP (classic) | rs1369766 |
| ClinGen | rs1369766 |
| ebi | rs1369766 |
| HLI | rs1369766 |
| Exac | rs1369766 |
| Gnomad | rs1369766 |
| Varsome | rs1369766 |
| LitVar | rs1369766 |
| Map | rs1369766 |
| PheGenI | rs1369766 |
| Biobank | rs1369766 |
| 1000 genomes | rs1369766 |
| hgdp | rs1369766 |
| ensembl | rs1369766 |
| geneview | rs1369766 |
| scholar | rs1369766 |
| rs1369766 | |
| pharmgkb | rs1369766 |
| gwascentral | rs1369766 |
| openSNP | rs1369766 |
| 23andMe | rs1369766 |
| SNPshot | rs1369766 |
| SNPdbe | rs1369766 |
| MSV3d | rs1369766 |
| GWAS Ctlg | rs1369766 |
| GMAF | 0.4426 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 17564975
] Autosomal dominant nonsyndromic cleft lip and palate: significant evidence of linkage at 18q21.1.
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 18
- Has genotype
- Has population
- Uses omim
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip Ancestry v2c
- On chip Ancestry v2d
