|
rs10510050
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In addition, rs10510050 was significantly correlated with thrombocytopenia, emesis and hepatotoxicity.
|
25732572 |
2015 |
|
rs160441
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Our findings firstly exhibit that rs218916 and rs160441 within lncRNA RP11-37B2.1 significantly associate with the occurrence of thrombocytopenia and suggest RP11-37B2.1 genetic variants are potential biosignatures for thrombocytopenia during anti-TB treatment.
|
30924187 |
2019 |
|
rs218916
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Our findings firstly exhibit that rs218916 and rs160441 within lncRNA RP11-37B2.1 significantly associate with the occurrence of thrombocytopenia and suggest RP11-37B2.1 genetic variants are potential biosignatures for thrombocytopenia during anti-TB treatment.
|
30924187 |
2019 |
|
rs7694379
|
|
|
0.010 |
GeneticVariation |
BEFREE |
SNPs rs342275, rs342293, rs11789898, rs17824620, and rs7694379 can be used as predictors of thrombocytopenia induced by lobaplatin-based chemotherapy in patients with advanced lung cancer in China.
|
31279707 |
2019 |
|
rs9574547
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The minor allele of rs9574547 was associated with a lower risk for thrombocytopenia (discovery cohort, odds ratio, 0.45, 95% confidence interval, 0.30-0.67, <i>p</i> = 9.76 × 10<sup>-5</sup>) with the overall association confirmed by meta-analysis (meta-<i>p</i> = 7.88 × 10<sup>-6</sup>).
|
30103242 |
2018 |
|
rs2274407
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The CA genotype of A934C (Lys304Asn) substitution correlated in contrast with lower event-free survival (P = .02) and higher frequency of high-grade thrombocytopenia (P = .01).
|
19515727 |
2009 |
|
rs766715154
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The CA genotype of A934C (Lys304Asn) substitution correlated in contrast with lower event-free survival (P = .02) and higher frequency of high-grade thrombocytopenia (P = .01).
|
19515727 |
2009 |
|
rs2231142
|
|
|
0.010 |
GeneticVariation |
BEFREE |
ABCG2 421C>A could explain part of the inter-individual variability of sunitinib-induced severe thrombocytopenia.
|
26914831 |
2016 |
|
rs1554785242
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs1554791280
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs1554800065
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
|
rs863223318
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders.
|
31064749 |
2019 |
|
rs28362731
|
|
|
0.010 |
GeneticVariation |
BEFREE |
AQP1 rs28362731 was significantly associated with thrombocytopenia (unadjusted: OR = 3.73, 95% CI = 1.00-13.84, P = 0.049; adjusted for pain: OR = 4.63, 95% CI = 1.13-19.05, P = 0.034) in additive model.
|
30840592 |
2019 |
|
rs11789898
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Single-nucleotide polymorphisms (rs342275, rs342293, rs7694379, rs11789898, and rs17824620) showed significant association with lobaplatin-induced thrombocytopenia.
|
31279707 |
2019 |
|
rs2290280
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In squamous cell carcinoma, rs4150558, rs2290280, rs8067195 were significantly associated with anemia, rs3786136 was significantly related to thrombocytopenia, ERCC5 presented consecutive significant signals in response rate.
|
28924235 |
2017 |
|
rs2287886
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The results suggest that rs2287886 G/G genotype of CD209 gene is associated with development of dengue requiring hospitalization while A/A genotype of rs735239 is associated with thrombocytopenia in dengue cases.
|
23624202 |
2013 |
|
rs735239
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The results suggest that rs2287886 G/G genotype of CD209 gene is associated with development of dengue requiring hospitalization while A/A genotype of rs735239 is associated with thrombocytopenia in dengue cases.
|
23624202 |
2013 |
|
rs1553196096
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs555607708
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs121908064
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders.
|
31064749 |
2019 |
|
rs121908065
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIbα (Bolzano mutation).
|
21933849 |
2012 |
|
rs757006129
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Our data show that the R307H SNP is significantly associated with the degree of thrombocytopenia in congenital and acquired platelet disorders, and may affect platelets by altering microtubule behavior.
|
25529050 |
2015 |
|
rs757788894
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
|
rs794727505
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders.
|
31064749 |
2019 |
|
rs2297630
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In this study, non-G group of rs2297630 in SDF1 significantly increased the risk of post-transplant thrombocytopenia in the first week of kidney transplantation.
|
31009686 |
2019 |