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. 2013 May 22;2013:937846. doi: 10.1155/2013/937846

Table 4.

SNP genotype association with alloimmunization in SCD.

SNP Gene Genotypes Number of patients* P value HapMap#
Antibody positive Antibody negative
(1) rs1049388 ARHG CC/CG/GG 21/8/0 21/11/0 0.593273 62/30/8
(2) rs1451724 ARHG AA/AG/GG 1/3/27 0/3/29 0.833054 0/23/77
(3) rs4910852 ARHG AA/AG/GG 25/7/0 18/10/0 0.264449 61/30/9
(4) rs7128013 ARHG AA/AC/CC 13/12/5 11/18/4 0.543399 25/49/26
(5) rs7929197 ARHG CC/CT/TT 7/13/12 8/12/5 0.429608 30/45/25
(6) rs10742177 ARHG CC/CG/GG 10/14/7 18/3/5 0.008979 41/45/14
(7) rs10835182 ARHG AA/AT/TT 0/14/15 0/12/20 0.444898 2/23/75
(8) rs10835184 ARHG AA/AT/TT 25/2/0 26/2/2 0.550071 95/5/0
(9) rs12272393 ARHG AA/AC/CC 7/13/14 8/12/11 0.817062 30/45/25
(10) rs17173879 ARHG AA/AG/GG 30/2/0 25/1/0 0.999999 93/7/0

(11) rs2231529 CHRNA CC/CT 27/3/1 35/2/0 0.493847 93/7/0
(12) rs2231532 CHRNA AA/AG/GG 19/13/3 14/12/5 0.609984 63/35/2
(13) rs2271583 CHRNA AA/AG/GG 4/14/15 2/9/18 0.422893 10/33/57
(14) rs2672213 CHRNA CC/CT/TT 30/2/0 23/4/0 0.397881 97/3/0
(15) rs2672216 CHRNA CC/CT/TT 32/2/0 25/8/1 0.062890 85/13/2
(16) rs2741862 CHRNA CC/CT/TT 5/25/4 14/14/5 0.022396 23/35/42
(17) rs12221525 CHRNA CC/CG/GG 20/8/4 20/11/2 0.562563 50/37/13

(18) rs708564** CD81 CC/CT/TT 5/15/11 23/8/3 0.000086 ## 82/17/2
(19) rs731909 CD81 CC/CG/GG 27/6/3 33/2/0 0.064002 90/8/2
(20) rs756915 CD81 CC/CT/TT 9/19/8 12/14/10 0.495260 21/50/29
(21) rs800137 CD81 CC/CT/TT 6/16/13 14/14/7 0.086688 46/31/24
(22) rs800335 CD81 CC/CT/TT 7/10/18 4/8/24 0.374866 82/17/2
(23) rs874330 CD81 CC/CT/TT 13/15/7 19/9/7 0.284287 52/40/8
(24) rs2019938 CD81 AA/AG/GG 11/13/5 15/14/8 0.851861 43/33/23
(25) rs2237863 CD81 CC/CT/TT 3/22/5 15/10/6 0.001518 ## 15/47/38
(26) rs11022565 CD81 GG/GT/TT 17/14/4 21/7/5 0.280369 61/32/7
(27) rs11022567 CD81 AA/AG/GG 5/14/16 5/7/25 0.120284 7/33/60

*Patient numbers are displayed in the order shown in the column labeled genotypes. #Relative distribution of genotypes in Sub-Saharan population, as reported by the HapMap. This research utilizes the NCBI SNP database [41], (http://www.ncbi.nih.gov/snp/). The Single Nucleotide Polymorphism database (dbSNP) is a public domain archive for a broad collection of simple genetic polymorphisms. dbSNP reports many cases of SNPs genotyped by HapMap and other projects which provide additional genotype and allele frequency information. **NCBI database describes two additional alleles, A/G with very low frequencies (<0.5%) for rs708564. This might be due to a mutational mechanism that leads to the simultaneous creation of two new base pairs at the same site which is beyond the scope of this study [42]. Our results, however, are based on the two reference SNPs alleles (C/T) of rs708564. ## P values significant comparing SCD patients with and without alloimmunization.