. Author manuscript; available in PMC: 2016 Dec 6.

Published in final edited form as: J Hum Genet. 2010 Nov 25;56(1):58–63. doi: 10.1038/jhg.2010.144

Table 3. Carrier frequency of rare and low-frequency variants in UK cases and controls.

ID	dbSNP	Major/minor allele	Cases^b	Controls^b	P-value
CCND1–3^a	rs36225071	G/C	0/150	1/222	0.60
CCND1–7	rs36225069	A/T	5/151	7/779	0.03
CCND1–10	rs36225073	G/A	8/146	35/743	0.67
CCND1–13	rs3212859	G/T	7/142	34/749	0.83
CCND1–15	rs954619	C/T	0/151	1/747	1.00
CCND1–17	NA	T/C	1/150	11/736	0.70
CCND1–18	NA	T/C	4/149	12/730	0.33
CCND1–19	rs55911137	G/C	1/107	0/732	0.13
CCND1–20	rs3862792	C/T	7/142	35/743	0.83
CCND1–22	NA	G/C	1/151	0/750	0.17
CCND1–27	rs3212906	T/A	2/146	9/720	1.00
CCND1–28	rs55666306	G/A	1/145	0/749	0.16
CCND1–29	rs3212907	C/T	10/147	70/747	0.43

Abbreviations: dbSNP, single nucleotide polymorphism database; NA, not available.

Typed in only 222 controls.

Number of cases or controls carrying the minor allele/total number of individuals successfully genotyped.