Table 2.
Polymorphism | rs# | Description | Minor/Major Allele | MAF | Missing Rate |
---|---|---|---|---|---|
ACE | rs1799752 | Intronic | I/D | 46% | 286 (3%) |
ACE −262 | rs4291 | 5' near gene | T/A | 37% | 205 (2%) |
ACE T776T | rs4343 | synonymous | G/A | 44% | 155 (2%) |
ACE 20320 | rs4363 | Intronic | G/A | 49% | 144 (2%) |
AGT −6 | rs5051 | 5' UTR | G/A | 42% | 152 (2%) |
AGT −20 | rs5050 | 5' UTR | C/A | 14% | 126 (1%) |
AGT M235T | rs699 | missense | T/C | 43% | 192 (2%) |
AGTR1 1166 | rs5186 | 3' UTR | C/A | 24% | 195 (2%) |
AGTR1 −535 | rs1492078 | 5' near gene | A/G | 48% | 291 (3%) |
AGTR1 −153 | rs275653 | 5' near gene | C/T | 19% | 158 (2%) |
α-Adducin G460T | rs4961 | missense | T/G | 16% | 199 (2%) |
GNB3 S825S | rs5443 | synonymous | T/C | 44% | 194 (2%) |
REN −1111 | rs6681776 | 3' near gene | A/G | 15% | 123 (1%) |
REN 2646 | rs2368564 | Intronic | T/C | 38% | 143 (1%) |
GRK4 R65L | rs2960306 | missense | T/G | 38% | 130 (1%) |
GRK4 A142V | rs1024323 | missense | T/C | 42% | 187 (2%) |
GRK4 A486V | rs1801058 | missense | T/C | 33% | 168 (2%) |
NPPA V664M | rs5063 | missense | A/G | 5% | 173 (2%) |
NPPA X2238R | rs5065 | missense | C/T | 22% | 180 (2%) |
SCNNIA T663A | rs2228576 | missense | A/G | 23% | 287 (3%) |
NOS3 E298D | rs1799983 | missense | T/G | 26% | 184 (2%) |
NOS3 −690 | rs3918226 | intronic | T/C | 7% | 172 (2%) |
NOS3 −922 | rs1800779 | intronic | G/A | 31% | 179 (2%) |
PON1 −108 | rs705379 | 3' near gene | T/C | 40% | 260 (3%) |