chr1:42742890:A>G Detail (hg38)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr1:43,208,561-43,208,561 View the variant detail on this assembly version. |
| hg38 | chr1:42,742,890-42,742,890 |
HGVS
[No Data.]
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
| JP | HGVD:[No Data.] |
| ToMMo:0.037 | |
| NCBN:[No Data.] | |
| NCBN(Hondo):[No Data.] | |
| NCBN(Ryukyu):[No Data.] | |
| East asia | ExAC:[No Data.] |
Prediction
ClinVar
| Clinical Significance | |
| Review star | [No Data.] |
| Show details | |
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
| Score | Disease name | Description | Source | Pubmed | Links |
|---|---|---|---|---|---|
| <0.001 | Diabetes Mellitus, Non-Insulin-Dependent | Among women with magnesium intake in the lowest 30% (AA: ≤0.164 g/d; HA: ≤0.185 ... | BeFree | 25733456 | Detail |
| <0.001 | Diabetes Mellitus, Non-Insulin-Dependent | Among women with magnesium intake in the lowest 30% (AA: ≤0.164 g/d; HA: ≤0.185 ... | BeFree | 25733456 | Detail |
| <0.001 | Diabetes Mellitus, Non-Insulin-Dependent | Among women with magnesium intake in the lowest 30% (AA: ≤0.164 g/d; HA: ≤0.185 ... | BeFree | 25733456 | Detail |
| 0.466 | Diabetes Mellitus, Non-Insulin-Dependent | Among women with magnesium intake in the lowest 30% (AA: ≤0.164 g/d; HA: ≤0.185 ... | BeFree | 25733456 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| Among women with magnesium intake in the lowest 30% (AA: ≤0.164 g/d; HA: ≤0.185 g/d), 4 SNP signals ... | DisGeNET | Detail |
| Among women with magnesium intake in the lowest 30% (AA: ≤0.164 g/d; HA: ≤0.185 g/d), 4 SNP signals ... | DisGeNET | Detail |
| Among women with magnesium intake in the lowest 30% (AA: ≤0.164 g/d; HA: ≤0.185 g/d), 4 SNP signals ... | DisGeNET | Detail |
| Among women with magnesium intake in the lowest 30% (AA: ≤0.164 g/d; HA: ≤0.185 g/d), 4 SNP signals ... | DisGeNET | Detail |
- Gene
- -
- dbSNP
- rs11590362 dbSNP
- Genome
- hg38
- Position
- chr1:42,742,890-42,742,890
- Variant Type
- snv
- Reference Allele
- A
- Alternative Allele
- G
- ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- PASS
- Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- rs11590362
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.0372
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 623
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
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