chr10:67883584:T>C Detail (hg38)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr10:69,643,342-69,643,342 View the variant detail on this assembly version. |
hg38 | chr10:67,883,584-67,883,584 |
HGVS
[No Data.]
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:0.179 | |
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 | Metabolic syndrome X | Nominally significant associations were also observed between T2D and the SIRT1 ... | BeFree | 20503258 | Detail |
0.211 | Diabetes Mellitus, Non-Insulin-Dependent | Nominally significant associations were also observed between T2D and the SIRT1 ... | BeFree | 20503258 | Detail |
0.204 | Metabolic syndrome X | Nominally significant associations were also observed between T2D and the SIRT1 ... | BeFree | 20503258 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
Nominally significant associations were also observed between T2D and the SIRT1 rs3758391 SNP and MS... | DisGeNET | Detail |
Nominally significant associations were also observed between T2D and the SIRT1 rs3758391 SNP and MS... | DisGeNET | Detail |
Nominally significant associations were also observed between T2D and the SIRT1 rs3758391 SNP and MS... | DisGeNET | Detail |
- Gene
- -
- dbSNP
- rs3758391 dbSNP
- Genome
- hg38
- Position
- chr10:67,883,584-67,883,584
- Variant Type
- snv
- Reference Allele
- T
- Alternative Allele
- C
- 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))
- rs3758391
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.1792
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 3003
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
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