chr19:34322137:A>G Detail (hg19)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr19:34,322,137-34,322,137 |
| hg38 | chr19:33,831,232-33,831,232 View the variant detail on this assembly version. |
HGVS
[No Data.]
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
| JP | HGVD:[No Data.] |
| ToMMo:0.286 | |
| 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 | Cardiovascular Diseases | Four polymorphisms (rs9939609 [FTO], rs11084753 [KCTD15], rs10838738 [MTCH2], an... | BeFree | 19910641 | Detail |
| <0.001 | Cardiovascular Diseases | Four polymorphisms (rs9939609 [FTO], rs11084753 [KCTD15], rs10838738 [MTCH2], an... | BeFree | 19910641 | Detail |
| <0.001 | Cardiovascular Diseases | Four polymorphisms (rs9939609 [FTO], rs11084753 [KCTD15], rs10838738 [MTCH2], an... | BeFree | 19910641 | Detail |
| 0.006 | Cardiovascular Diseases | Four polymorphisms (rs9939609 [FTO], rs11084753 [KCTD15], rs10838738 [MTCH2], an... | BeFree | 19910641 | Detail |
| 0.153 | obesity | After adjusting for age, sex and multiple testing, MC4R rs17782313, SEC16B rs543... | BeFree | 25637721 | Detail |
| 0.121 | obesity | After adjusting for age, sex and multiple testing, MC4R rs17782313, SEC16B rs543... | BeFree | 25637721 | Detail |
| 0.021 | obesity | After adjusting for age, sex and multiple testing, MC4R rs17782313, SEC16B rs543... | BeFree | 25637721 | Detail |
| 0.791 | obesity | After adjusting for age, sex and multiple testing, MC4R rs17782313, SEC16B rs543... | BeFree | 25637721 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| Four polymorphisms (rs9939609 [FTO], rs11084753 [KCTD15], rs10838738 [MTCH2], and rs10938397 [GNPDA2... | DisGeNET | Detail |
| Four polymorphisms (rs9939609 [FTO], rs11084753 [KCTD15], rs10838738 [MTCH2], and rs10938397 [GNPDA2... | DisGeNET | Detail |
| Four polymorphisms (rs9939609 [FTO], rs11084753 [KCTD15], rs10838738 [MTCH2], and rs10938397 [GNPDA2... | DisGeNET | Detail |
| Four polymorphisms (rs9939609 [FTO], rs11084753 [KCTD15], rs10838738 [MTCH2], and rs10938397 [GNPDA2... | DisGeNET | Detail |
| After adjusting for age, sex and multiple testing, MC4R rs17782313, SEC16B rs543874, MAP2K5 rs224142... | DisGeNET | Detail |
| After adjusting for age, sex and multiple testing, MC4R rs17782313, SEC16B rs543874, MAP2K5 rs224142... | DisGeNET | Detail |
| After adjusting for age, sex and multiple testing, MC4R rs17782313, SEC16B rs543874, MAP2K5 rs224142... | DisGeNET | Detail |
| After adjusting for age, sex and multiple testing, MC4R rs17782313, SEC16B rs543874, MAP2K5 rs224142... | DisGeNET | Detail |
- Gene
- -
- dbSNP
- rs11084753 dbSNP
- Genome
- hg19
- Position
- chr19:34,322,137-34,322,137
- 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))
- rs11084753
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.2856
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 4786
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
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