chr6:152287367:T>C Detail (hg19) (ESR1)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr6:152,287,367-152,287,367 |
hg38 | chr6:151,966,232-151,966,232 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_000125.3:c.1096+21724T>C | |
NM_001122741.1:c.1096+21724T>C | ||
NM_001291230.1:c.1096+21724T>C |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:0.452 | |
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 |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.003 | dementia | Significant association was found between ESR1 polymorphisms (rs9340799 [ESR1+35... | BeFree | 23567436 | Detail |
<0.001 | Mild dementia | Significant association was found between ESR1 polymorphisms (rs9340799 [ESR1+35... | BeFree | 23567436 | Detail |
<0.001 | Mild dementia | Significant association was found between ESR1 polymorphisms (rs9340799 [ESR1+35... | BeFree | 23567436 | Detail |
0.012 | dementia | Significant association was found between ESR1 polymorphisms (rs9340799 [ESR1+35... | BeFree | 23567436 | Detail |
0.002 | Presenile dementia | Significant association was found between ESR1 polymorphisms (rs9340799 [ESR1+35... | BeFree | 23567436 | Detail |
0.003 | Presenile dementia | Significant association was found between ESR1 polymorphisms (rs9340799 [ESR1+35... | BeFree | 23567436 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
Significant association was found between ESR1 polymorphisms (rs9340799 [ESR1+351], rs1801132 [ESR1+... | DisGeNET | Detail |
Significant association was found between ESR1 polymorphisms (rs9340799 [ESR1+351], rs1801132 [ESR1+... | DisGeNET | Detail |
Significant association was found between ESR1 polymorphisms (rs9340799 [ESR1+351], rs1801132 [ESR1+... | DisGeNET | Detail |
Significant association was found between ESR1 polymorphisms (rs9340799 [ESR1+351], rs1801132 [ESR1+... | DisGeNET | Detail |
Significant association was found between ESR1 polymorphisms (rs9340799 [ESR1+351], rs1801132 [ESR1+... | DisGeNET | Detail |
Significant association was found between ESR1 polymorphisms (rs9340799 [ESR1+351], rs1801132 [ESR1+... | DisGeNET | Detail |
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs1884049 dbSNP
- Genome
- hg19
- Position
- chr6:152,287,367-152,287,367
- 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))
- rs1884049
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.4517
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 7571
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
Genome browser