Source: BEFREE ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17427960
rs17427960
Entrez Id: 100316868
Gene Symbol: HOTTIP
HOTTIP
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE The results showed three SNPs (rs3807598, rs2067087, and rs17427960) were associated with enhanced CRC risk both in overall and stratified analysis. 30940774 2019
dbSNP: rs17501292
rs17501292
Entrez Id: 3209;100316868
Gene Symbol: HOXA13;HOTTIP
HOXA13;HOTTIP
CUI: C0027651
Disease:
Neoplasms
0.010 GeneticVariation BEFREE One polymorphism, rs17501292, could improve the overall survival (OS) of CRC patients in the tumor of ulcerative/invasive-type subgroup. 30940774 2019
dbSNP: rs2067087
rs2067087
Entrez Id: 3209;100316868
Gene Symbol: HOXA13;HOTTIP
HOXA13;HOTTIP
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE The results showed three SNPs (rs3807598, rs2067087, and rs17427960) were associated with enhanced CRC risk both in overall and stratified analysis. 30940774 2019
dbSNP: rs17427960
rs17427960
Entrez Id: 100316868
Gene Symbol: HOTTIP
HOTTIP
CUI: C2239176
Disease:
Liver carcinoma
0.010 GeneticVariation BEFREE The <i>HOTTIP</i> rs17501292, rs2067087, and rs17427960 SNPs were increased to 1.55-, 1.20-, and 1.18-fold HCC risk under allelic models (<i>P</i> = 0.012, 0.017 and 0.049, respectively). 29930469 2018
dbSNP: rs17501292
rs17501292
Entrez Id: 3209;100316868
Gene Symbol: HOXA13;HOTTIP
HOXA13;HOTTIP
CUI: C2239176
Disease:
Liver carcinoma
0.010 GeneticVariation BEFREE In addition, the two-way interaction of <i>HOTTIP</i> rs17501292-<i>MALAT1</i> rs619586 polymorphisms showed a decreased effect on HCC risk (<i>P</i><sub>interaction</sub> = 0.028, OR = 0.30) and epistasis with each other. 29930469 2018
dbSNP: rs1859168
rs1859168
Entrez Id: 100316868
Gene Symbol: HOTTIP
HOTTIP
CUI: C1306459
Disease:
Primary malignant neoplasm
0.010 GeneticVariation BEFREE Our study also demonstrated that other SNPs were correlated with overall cancer risk, namely, metastasis-associated lung adenocarcinoma transcript 1 (MALAT1, rs619586 A/G), HOXA distal transcript antisense RNA (HOTTIP, rs1859168 A/C), and highly up-regulated in liver cancer (HULC, rs7763881 A/C). 29802154 2018
dbSNP: rs1859168
rs1859168
Entrez Id: 100316868
Gene Symbol: HOTTIP
HOTTIP
CUI: C0699791
Disease:
Stomach Carcinoma
0.010 GeneticVariation BEFREE Our findings showed rs4784659, rs579501 and rs1859168 reduced the susceptibility of gastric cancer. 29305976 2018
dbSNP: rs1859168
rs1859168
Entrez Id: 100316868
Gene Symbol: HOTTIP
HOTTIP
CUI: C0024623
Disease:
Malignant neoplasm of stomach
0.010 GeneticVariation BEFREE Our findings showed rs4784659, rs579501 and rs1859168 reduced the susceptibility of gastric cancer. 29305976 2018
dbSNP: rs1859168
rs1859168
Entrez Id: 100316868
Gene Symbol: HOTTIP
HOTTIP
CUI: C0006826
Disease:
Malignant Neoplasms
0.010 GeneticVariation BEFREE Our study also demonstrated that other SNPs were correlated with overall cancer risk, namely, metastasis-associated lung adenocarcinoma transcript 1 (MALAT1, rs619586 A/G), HOXA distal transcript antisense RNA (HOTTIP, rs1859168 A/C), and highly up-regulated in liver cancer (HULC, rs7763881 A/C). 29802154 2018
dbSNP: rs2071265
rs2071265
Entrez Id: 3209;100316868
Gene Symbol: HOXA13;HOTTIP
HOXA13;HOTTIP
CUI: C2239176
Disease:
Liver carcinoma
0.010 GeneticVariation BEFREE HOTTIP rs2071265 is associated with an earlier recurrence in HCC patients. 30652087 2018
dbSNP: rs1859168
rs1859168
Entrez Id: 100316868
Gene Symbol: HOTTIP
HOTTIP
CUI: C0346647
Disease:
Malignant neoplasm of pancreas
0.010 GeneticVariation BEFREE The current findings provided evidence that the functional rs1859168 A > C polymorphism may decrease the PC risk by down-regulating the HOTTIP expression. 28818070 2017
dbSNP: rs1859168
rs1859168
Entrez Id: 100316868
Gene Symbol: HOTTIP
HOTTIP
CUI: C0235974
Disease:
Pancreatic carcinoma
0.010 GeneticVariation BEFREE The current findings provided evidence that the functional rs1859168 A > C polymorphism may decrease the PC risk by down-regulating the HOTTIP expression. 28818070 2017
dbSNP: rs1859168
rs1859168
Entrez Id: 100316868
Gene Symbol: HOTTIP
HOTTIP
CUI: C1306460
Disease:
Primary malignant neoplasm of lung
0.010 GeneticVariation BEFREE We found that patients with HOTTIP rs5883064 C allele or rs1859168 A allele had increased lung cancer risk (P = 0.01, P = 0.01, respectively). 26729200 2016
dbSNP: rs1859168
rs1859168
Entrez Id: 100316868
Gene Symbol: HOTTIP
HOTTIP
CUI: C0684249
Disease:
Carcinoma of lung
0.010 GeneticVariation BEFREE We found that patients with HOTTIP rs5883064 C allele or rs1859168 A allele had increased lung cancer risk (P = 0.01, P = 0.01, respectively). 26729200 2016
dbSNP: rs1859168
rs1859168
Entrez Id: 100316868
Gene Symbol: HOTTIP
HOTTIP
CUI: C0242379
Disease:
Malignant neoplasm of lung
0.010 GeneticVariation BEFREE We found that patients with HOTTIP rs5883064 C allele or rs1859168 A allele had increased lung cancer risk (P = 0.01, P = 0.01, respectively). 26729200 2016
dbSNP: rs5883064
rs5883064
Entrez Id: 100316868
Gene Symbol: HOTTIP
HOTTIP
CUI: C0242379
Disease:
Malignant neoplasm of lung
0.010 GeneticVariation BEFREE We found that patients with HOTTIP rs5883064 C allele or rs1859168 A allele had increased lung cancer risk (P = 0.01, P = 0.01, respectively). 26729200 2016
dbSNP: rs5883064
rs5883064
Entrez Id: 100316868
Gene Symbol: HOTTIP
HOTTIP
CUI: C1306460
Disease:
Primary malignant neoplasm of lung
0.010 GeneticVariation BEFREE We found that patients with HOTTIP rs5883064 C allele or rs1859168 A allele had increased lung cancer risk (P = 0.01, P = 0.01, respectively). 26729200 2016
dbSNP: rs5883064
rs5883064
Entrez Id: 100316868
Gene Symbol: HOTTIP
HOTTIP
CUI: C0684249
Disease:
Carcinoma of lung
0.010 GeneticVariation BEFREE We found that patients with HOTTIP rs5883064 C allele or rs1859168 A allele had increased lung cancer risk (P = 0.01, P = 0.01, respectively). 26729200 2016