Skip to main content
. 2023 Jun 16;62(1):229–241. doi: 10.1007/s10528-023-10418-5

Table 2.

Genotype and allele frequencies of two H19 SNPs in study groups by gender (n, %)

Genotypes/Alleles of rs2839698 Genotypes/Alleles of rs217727
C/C C/T T/T χ2 P C T χ2 P C/C C/T T/T χ2 P C T χ2 P
Normal controls
 Males (n = 99) 50 (50.5) 35 (35.4) 14 (14.1) 135 (68.2) 63 (31.8) 37 (37.4) 52 (52.5) 10 (10.1) 126 (63.6) 72 (36.4)
 Females (n = 293) 153 (52.5) 118 (40.3) 22 (7.5) 424 (72.4) 162 (27.6) 144 (49.1) 124 (42.3) 25 (8.5) 412 (70.3) 174 (29.7)
 Total (n = 392) 203 (51.8) 153 (39) 36 (9.2) 559 (71.3) 225 (28.7) 181 (46.2) 176 (44.9) 35 (8.9) 538 (68.9) 246 (31.4)
Obese group
 Males (n = 54) 4 (7.4) 34 (63) 16 (29.6) 28.5 <0.0001 42 (38.9) 66 (61.1) 24.6 <0.0001 34 (63) 18 (33.3) 2 (3.7) 9.56 0.008 86 (79.6) 22 (20.4) 10.6 0.001
 Females (n = 360) 35 (9.7) 244 (67.8) 81 (22.5) 146 <0.0001 314 (43.6) 406 (56.4) 108 <0.0001 212 (58.9) 139 (38.6) 9 (2.5) 14.6 0.001 563 (78.2) 157 (21.8) 8.4 0.004
 Total (n = 414) 39 (9.4) 278 (67.1) 97 (23.4) 175 <0.0001 356 (43) 472 (57) 132 <0.0001 246 (59.4) 157 (37.9) 11 (2.7) 22.9 <0.0001 649 (78.4) 179 (21.6) 19.7 <0.0001

According to the SNP database, the wildtype alleles for both rs2839698 and rs217727 are C on minus strand. The T alleles were the minor allele for both SNPs and considered as effect alleles

C/C, homozygous reference; C/T, heterozygous and T/T, homozygous mutant for rs2839698 SNP (based on SNP database)

C/C, homozygous reference; C/T, heterozygous and T/T, homozygous mutant for rs217727 SNPs (based on SNP database)

Genotype frequencies are shown in parentheses. χ2 test and P value are presented for obese groups vs. normal BMI control subjects