rs623155
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs623155(A;A) |
| Make rs623155(A;G) |
| Make rs623155(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 6 |
| Position | 78557764 |
| Gene | LOC105377865 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs623155 |
| dbSNP (classic) | rs623155 |
| ClinGen | rs623155 |
| ebi | rs623155 |
| HLI | rs623155 |
| Exac | rs623155 |
| Gnomad | rs623155 |
| Varsome | rs623155 |
| LitVar | rs623155 |
| Map | rs623155 |
| PheGenI | rs623155 |
| Biobank | rs623155 |
| 1000 genomes | rs623155 |
| hgdp | rs623155 |
| ensembl | rs623155 |
| geneview | rs623155 |
| scholar | rs623155 |
| rs623155 | |
| pharmgkb | rs623155 |
| gwascentral | rs623155 |
| openSNP | rs623155 |
| 23andMe | rs623155 |
| SNPshot | rs623155 |
| SNPdbe | rs623155 |
| MSV3d | rs623155 |
| GWAS Ctlg | rs623155 |
| GMAF | 0.4665 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
A study in Arab families found that an autosomal dominant condition known as split hand/foot malformation with long bone deficiency 2 (SHFLD2) maps between two SNPs, rs623155 and rs1547251. (Variation at these two SNPs themselves does not appear to cause split hand.) OMIM
[PMID 17160898
] Genomewide linkage scan for split-hand/foot malformation with long-bone deficiency in a large Arab family identifies two novel susceptibility loci on chromosomes 1q42.2-q43 and 6q14.1.
