chr12:12715152:G>A Detail (hg38)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr12:12,868,086-12,868,086 View the variant detail on this assembly version. |
hg38 | chr12:12,715,152-12,715,152 |
HGVS
[No Data.]
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:0.458 | |
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 | Malignant neoplasm of endometrium | Three single nucleotide polymorphisms in the CDKN1B gene (rs11055027, rs3759216,... | BeFree | 21454826 | Detail |
0.002 | endometrial carcinoma | Three single nucleotide polymorphisms in the CDKN1B gene (rs11055027, rs3759216,... | BeFree | 21454826 | Detail |
0.001 | uterine corpus cancer | Three single nucleotide polymorphisms in the CDKN1B gene (rs11055027, rs3759216,... | BeFree | 21454826 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
Three single nucleotide polymorphisms in the CDKN1B gene (rs11055027, rs3759216, and rs34330) were r... | DisGeNET | Detail |
Three single nucleotide polymorphisms in the CDKN1B gene (rs11055027, rs3759216, and rs34330) were r... | DisGeNET | Detail |
Three single nucleotide polymorphisms in the CDKN1B gene (rs11055027, rs3759216, and rs34330) were r... | DisGeNET | Detail |
- Gene
- -
- dbSNP
- rs3759216 dbSNP
- Genome
- hg38
- Position
- chr12:12,715,152-12,715,152
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- A
- 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))
- rs3759216
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.4584
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 7682
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
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