Table 1 Single‐nucleotide polymorphisms selected from within the MYH9 locus and their relative transmission disequilibrium test results.

n	dbSNP id	Genome position*	bp to next	Gene position	Alleles†	MAF‡	T/NT§	p Value¶
1	rs5995288	chr22:35087134	16555	Intron 1	G/A	0.36	91/88	0.82
2	rs739097	chr22:35070579	27221	Intron 1	T/C	0.49	85/94	0.50
3	rs2071731	chr22:35043358	4199	Intron 6	C/T	0.41	93/95	0.88
4	rs1002246	chr22:35039159	4476	Intron 10	C/T	0.29	81/81	1.00
5	rs3752462	chr22:35034683	10877	Intron 13	G/A	0.41	84/116	0.02
6	rs2009930	chr22:35023806	14952	Intron 19	T/C	0.40	95/107	0.40
7	rs2269529	chr22:35008854	6440	Exon 33	A/G	0.26	78/83	0.69
8	rs7078	chr22:35002414	—	Exon.40‐3′UTR	T/C	0.29	72/84	0.34

MAF, minor allele frequency; SNP, single‐nucleotide polymorphism; T/NT, transmission/non‐transmission; UTR, untranslated.

*UCSC Genome Browser on Human May 2004 Assembly.

†SNP alleles in coding frame, major allele first.

‡MAF calculated from all parental chromosomes.

§T/NT counts from heterozygous parents are given for the major allele.

¶p value for transmission disequilibrium test.