eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| hepatitis a | ||||
| Disease ID | 1487 |
|---|---|
| Disease | hepatitis a |
| Manually Symptom | (Waiting for update.) |
| Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:1) |
Manually Genotype(Total Text Mining Genotypes:0) |
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| (Waiting for update.) |
Text Mining Genotype(Total Genotypes:0) | |
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| (Waiting for update.) | |
All Snps(Total Genotypes:8) | |||||||||||||
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| snpId | pubmedId | geneId | geneSymbol | diseaseId | sourceId | sentence | score | Year | geneSymbol_dbSNP | CHROMOSOME | POS | REF | ALT |
| rs1042522 | 23564481 | 7157 | TP53 | umls:C0019159 | BeFree | Subgroup analyses by source of controls and hepatitis virus infection status further demonstrated the significant association, whereas stratification factors involving gender and family history of HCC did not modify the association between p53 codon 72 Arg/Pro polymorphism and HCC risk. | 0.003257302 | 2013 | TP53 | 17 | 7676154 | G | T,C |
| rs10853728 | 23469142 | 3627 | CXCL10 | umls:C0019159 | BeFree | In HBeAg-positive patients (n = 48), HBV viral load correlated with active hepatitis, while in HBeAg-negative patients (n = 67), rs10853728 CC genotype (p = 0.032) and a trend of higher IP-10 levels (p = 0.092) were associated with active hepatitis. | 0.000814326 | 2013 | NA | 19 | 39254506 | C | G,T |
| rs11540654 | 23564481 | 7157 | TP53 | umls:C0019159 | BeFree | Subgroup analyses by source of controls and hepatitis virus infection status further demonstrated the significant association, whereas stratification factors involving gender and family history of HCC did not modify the association between p53 codon 72 Arg/Pro polymorphism and HCC risk. | 0.003257302 | 2013 | TP53 | 17 | 7676040 | C | T,G,A |
| rs12979860 | 24085431 | 282617 | IFNL3 | umls:C0019159 | BeFree | In the overall analysis, the IL-28B rs12979860 T/C polymorphism was identified as a genetic risk factor for hepatitis virus-related HCC and LC development. | 0.001628651 | 2014 | IFNL3;IFNL4 | 19 | 39248147 | C | T |
| rs12979860 | 25971683 | 282617 | IFNL3 | umls:C0019159 | BeFree | Differential distribution of IL28B.rs12979860 single-nucleotide polymorphism among Egyptian healthcare workers with and without a hepatitis C virus-specific cellular immune response. | 0.001628651 | 2015 | IFNL3;IFNL4 | 19 | 39248147 | C | T |
| rs25487 | 23780894 | 7515 | XRCC1 | umls:C0019159 | BeFree | Our meta-analysis of the available data did not find an obvious effect of XRCC1 Arg399Gln polymorphism on hepatitis-related hepatocellular carcinoma. | 0.000814326 | 2013 | XRCC1 | 19 | 43551574 | T | C |
| rs386493716 | 23780894 | 7515 | XRCC1 | umls:C0019159 | BeFree | Our meta-analysis of the available data did not find an obvious effect of XRCC1 Arg399Gln polymorphism on hepatitis-related hepatocellular carcinoma. | 0.000814326 | 2013 | NA | NA | NA | NA | NA |
| rs386545618 | 24155211 | 4524 | MTHFR | umls:C0019159 | BeFree | Associations between MTHFR Ala222Val polymorphism and risks of hepatitis and hepatitis-related liver cancer: a meta-analysis. | 0.000271442 | 2013 | NA | NA | NA | NA | NA |
GWASdb Annotation(Total Genotypes:0) | |
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| (Waiting for update.) | |
GWASdb Snp Trait(Total Genotypes:0) | |
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| (Waiting for update.) | |
Mapped by lexical matching(Total Items:0) |
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| (Waiting for update.) |
Mapped by homologous gene(Total Items:0) |
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| (Waiting for update.) |
| Disease ID | 1487 |
|---|---|
| Disease | hepatitis a |
| Case | (Waiting for update.) |