Table 2.

NTRK2 single nucleotide polymorphisms (SNPs) used for genotyping.

	Identification Number
SNP	NCBI	Celera	Variation	Nucleotide positiona
1*	rs1147198	hCV7424042	C/A	84504902
2 (LNG5)	NRb	NR	A/G	84514790
3	rs1187325	hCV3237596	G/C	84515149
4 (LNG7)	NR	NR	T/C	84515449
5*	rs993315	hCV7424005	T/C	84517275
6*	rs1187352	hCV3237603	A/G	84523011
7*	rs1619120	hCV7423969	T/C	84531750
8	NR	hCV3237607	T/C	84533719
9	NR	hCV26567668	C/T	84545393
10	rs7041260	hCV2121698	C/G	84548082
11*	rs1778934	hCV2121705	G/A	84554176
12*	rs10081630	hCV2121711	T/A	84558452
13*	rs2489162	hCV2121715	C/T	84563296
14*	rs3780632	hCV11868468	C/T	84582342
15*	rs7048278	hCV25649147	G/A	84589707
16	rs7027979	hCV11868452	C/G	84610105
17*	rs1573219	hCV7422086	T/C	84617176
18*	rs12555159	hCV7958799	A/G	84624386
19	rs1443444	hCV7958706	C/T	84638865
20	rs3739804	hCV7958645	G/A	84651185
21*	rs1624327	hCV7958636	T/C	84658844
22	NR	hCV7958628	C/T	84664800
23*	rs1036914	hCV7958610	C/T	84667713
24*	rs11140776	hCV1231292	G/T	84676481
25	rs11140777	hCV1231291	C/T	84676515
26*	rs10868229	hCV26567734	G/A	84693116
27*	rs1822420	hCV11923616	T/C	84696830
28*	rs10780690	hCV7958556	T/G	84707726
29*	rs3780634	hCV1231360	G/A	84718272
30*	rs10780691	hCV1231358	C/T	84720807
31	rs11788168	hCV1231354	A/T	84729983
32	rs736744	hCV1231348	A/G	84743961
33*	rs4304401	hCV26566813	T/C	84760065
34*	rs920776	hCV7423761	T/C	84767890
35*	rs1078947	hCV581246	C/T	84792806
36	rs2277192	hCV7958330	G/A	84803531
37	rs10746752	hCV185062	A/G	84825270
38*	rs4504715	hCV185068	A/G	84829632
39*	rs4242630	hCV237788	C/T	84841099
40	rs1565445	hCV1935385	C/T	84846625
41*	rs1490404	hCV1935396	C/T	84852084
42	rs729560	hCV946149	G/A	84863859
43*	rs1490403	hCV1935405	A/T	84868060

^aHapMap NCBI Build 35.

^bNo record in database.

^*In addition to our genotyping results, genotypes and allele frequency data were available for these markers from HapMap Public Release #20 for the Utah sample from the Centre d’Etude du Polymorphisme Humain collection (CEU).