|
rs104893689
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
[Percutaneous tenotomy of achilles tendon in the treatment of congenital clubfeet--a preliminary report].
|
15751724 |
2004 |
|
rs104893689
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
In vivo and in vitro characterization of neonatal hyperparathyroidism resulting from a de novo, heterozygous mutation in the Ca2+-sensing receptor gene: normal maternal calcium homeostasis as a cause of secondary hyperparathyroidism in familial benign hypocalciuric hypercalcemia.
|
9011580 |
1997 |
|
rs104893689
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Expression and characterization of inactivating and activating mutations in the human Ca2+o-sensing receptor.
|
8702647 |
1996 |
|
rs104893689
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
A comparison of the abilities of typical neuroleptic agents and of thioridazine, clozapine, sulpiride and metoclopramide to antagonise the hyperactivity induced by dopamine applied intracerebrally to areas of the extrapyramidal and mesolimbic systems.
|
791660 |
1976 |
|
rs104893851
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs1057518886
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs116928232
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
|
rs1553454436
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs1555206402
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs1557607997
|
|
GC |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs1569548274
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs780533096
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
|
rs886037774
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
|
rs886037775
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
|
rs1695
|
|
|
0.010 |
GeneticVariation |
BEFREE |
GSTP1 c.313A>G genotype was recently described as a predictor of vomiting related to high-dose cisplatin.
|
30870506 |
2019 |
|
rs1799801
|
|
|
0.010 |
GeneticVariation |
BEFREE |
GSTP1 c.313A>G, XPD c.934G>A, XPF c.2505T>C and CASP9 c.-1339A>G Polymorphisms and Severity of Vomiting in Head and Neck Cancer Patients treated with Cisplatin Chemoradiation.
|
28686330 |
2017 |
|
rs324420
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We found significant FAAH-morphine interaction for missense (rs324420) and several regulatory variants, with HCVR (p < 0.0001) and vomiting (p = 0.0339).
|
27977335 |
2017 |
|
rs4818
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The COMT rs4818 polymorphism may prove useful in predicting emesis medication use postoperatively.
|
25185591 |
2014 |
|
rs639174
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Among the results found, we detected for the first time an association between rs639174 in DROSHA and vomits that remained statistically significant after FDR correction.
|
24614921 |
2014 |
|
rs1062613
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Those with genotypes associated with increased expression of the 5-HT3A receptor subunit (rs1062613, CT or TT) had worse final PUQE scores (p = 0.01) than other subjects while rs3782025 variants carriers had significantly better initial (p = 0.02) and final (p = 0.02) PUQE scores than other subjects.
|
23786674 |
2013 |
|
rs267607165
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Thus, the E410K substitution defines a new genetic aetiology for Moebius syndrome, Kallmann syndrome and cyclic vomiting.
|
23378218 |
2013 |
|
rs3758987
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The HTR3B rs3758987 SNP might serve as a predictor of post-operative vomiting in Chinese Han patients undergoing gynaecological laparoscopic surgery.
|
23464988 |
2013 |
|
rs3782025
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Those with genotypes associated with increased expression of the 5-HT3A receptor subunit (rs1062613, CT or TT) had worse final PUQE scores (p = 0.01) than other subjects while rs3782025 variants carriers had significantly better initial (p = 0.02) and final (p = 0.02) PUQE scores than other subjects.
|
23786674 |
2013 |
|
rs77931234
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We suggest that in MCADD (1) a newborn screening C8 level of 6micromol/L or greater represents particular risk of sudden death; (2) that MCAD genotypes other than homozygosity for the c.985A>G mutation are also associated with sudden death; (3) that vomiting is a frequent symptom preceding sudden death; and (4) social support and medical follow-up of these families are crucial in reducing the occurrence of sudden death.
|
20580581 |
2010 |
|
rs6766410
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The variant genotype of K163N (HTR3C) was associated with vomiting, which occurred in 50.0% (P = 0.009).
|
18389280 |
2008 |