chr21:35525560:A>G Detail (hg38)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr21:36,897,858-36,897,858 View the variant detail on this assembly version. |
hg38 | chr21:35,525,560-35,525,560 |
HGVS
[No Data.]
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:0.262 | |
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 | Through an exhaustive search of pair-wise interactions and a selected search of ... | BeFree | 23626757 | Detail |
<0.001 | Diabetes Mellitus, Non-Insulin-Dependent | Through an exhaustive search of pair-wise interactions and a selected search of ... | BeFree | 23626757 | Detail |
0.341 | Diabetes Mellitus, Non-Insulin-Dependent | Through an exhaustive search of pair-wise interactions and a selected search of ... | BeFree | 23626757 | Detail |
<0.001 | Diabetes Mellitus, Non-Insulin-Dependent | Through an exhaustive search of pair-wise interactions and a selected search of ... | BeFree | 23626757 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
Through an exhaustive search of pair-wise interactions and a selected search of three- to five-way i... | DisGeNET | Detail |
Through an exhaustive search of pair-wise interactions and a selected search of three- to five-way i... | DisGeNET | Detail |
Through an exhaustive search of pair-wise interactions and a selected search of three- to five-way i... | DisGeNET | Detail |
Through an exhaustive search of pair-wise interactions and a selected search of three- to five-way i... | DisGeNET | Detail |
- Gene
- -
- dbSNP
- rs445984 dbSNP
- Genome
- hg38
- Position
- chr21:35,525,560-35,525,560
- 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))
- rs445984
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.2621
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 4393
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
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