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|
rs#
|
Gene
|
Variant
|
MAF
|
HWE
|
Genotypes
|
P
|
Alleles
|
P
|
|---|
|
Wild-type (case/con)
|
Hetero (case/con)
|
Homo (case/con)
|
Major (case/con)
|
Minor (case/con)
|
|---|
|
rs17796714
|
CARMN
|
G > A
|
0.31
|
0.86
|
25/97
|
22/86
|
10/15
|
0.08
|
72/282
|
42/116
|
0.12
|
|
rs13234328
|
TNRC18
|
G > A
|
0.23
|
0.36
|
37/112
|
16/79
|
4/7
|
0.18
|
90/303
|
24/93
|
0.59
|
|
rs1333114
|
PTPRD
|
G > A
|
0.37
|
0.92
|
29/72
|
24/94
|
4/32
|
0.07
|
82/238
|
32/158
|
0.02
|
|
rs11232965
|
MIR4300HG
|
T > C
|
0.42
|
0.44
|
29/58
|
20/99
|
8/41
|
0.01
|
78/215
|
36/181
|
0.007
|
- Incidences are presented as number
- rs# SNP identifier at dbSNP, MAF minor allele frequency, HWE p value of deviance from Hardy–Weinberg equilibrium, Hetero heterozygous mutant, Homo homozygous mutant, Major major allele, Minor minor allele, case patients with PONV, con patients without PONV, P p values in statistics
