No evidence for association between polymorphisms in GRM3and schizophrenia

BMC Psychiatry

Table 1 GRM3 single marker data

		n	11	12	22	p-value	1	2	p-value
rs187993	case	590	303	228	59	0.06	834 (0.71)	346 (0.29)	0.11
T/G	control	637	287	288	62		862 (0.68)	412 (0.32)
rs13242038	case	660	431	213	16	0.19	1075 (0.81)	245 (0.19)	0.60
C/T	control	703	460	214	29		1134 (0.81)	272 (0.19)
rs917071	case	659	337	272	50	0.61	946 (0.72)	372 (0.28)	0.33
C/T	control	697	373	278	46		1024 (0.73)	370 (0.27)
rs6465084	case	666	375	246	45	0.93	996 (0.75)	336 (0.25)	0.73
A/G	control	708	406	255	47		1067 (0.75)	349 (0.25)
rs2228595	case	663	561	98	4	0.85	1220 (0.92)	106 (0.08)	0.64
C/T	control	705	602	100	3		1304 (0.92)	106 (0.08)
rs1468412	case	663	345	264	54	0.68	954 (0.72)	372 (0.28)	0.41
A/T	control	698	375	274	49		1024 (0.73)	372 (0.27)
rs7804100	case	652	363	250	39	0.63	976 (0.75)	328 (0.25)	0.46
G/A	control	704	401	269	34		1071 (0.76)	337 (0.24)

Genotype and allele counts are shown for each SNP. Allele frequencies are shown in brackets. Minor alleles are coded as 2, using coding strand format as per Egan et al., [6]. For comparison between studies, rs2228595 was identified by Marti et al., [8] as +1131C>T and is referred to as snp5 in Egan et al., [6]. rs13242038, rs6465084 and rs7804100 are referred to as hCV2627921, hCV11245618 and hCV2536213 respectively in Egan et al., [6].

ISSN: 1471-244X