. 2005 Aug 10;77(4):567–581. doi: 10.1086/468189

Table 2.

SNPs Identified through Resequencing in 48 Patients with RA

dbSNP ID	SNP^a	Position^b	Type
rs1217419		C10488019A	Intron
ss38346956		A10487866T	Intron
ss38346953		A10487850T	Intron
ss38346954		A10487465G	Intron
rs1217418		T10487346C	Intron
rs1217417	7	C10487019G	Intron
rs1217416		G10486919A	TFBS
rs11582409		A10485548G	TFBS
ss38346952		G10484936C	Intron
ss38346955		A10484227G	Intron
rs3789609	8	A10483914G	Intron
rs3789608		A10483903G	Intron
ss38346947	9	T10483780C	Nonsense
ss38346946	10	A10483096T	Intron
rs2476602	11	T10483070C	Intron
rs1217410	12	G10482931A	Intron
ss38346945	14	A10480804G	Missense
rs3765598	15	A10480578G	Intron
ss38346951		T10477441A	Intron
ss38346957		C10477397G	Intron
ss38346950		A10466290T	Intron
rs17509844		T10463884C	Intron
rs2476601	22	T10463683C	Missense
ss38346944	23	T10463342G	Intron
rs1970559	24	G10463263A	Intron
rs2797415	25	T10463208C	Intron
rs3761935		C10458643A	Intron
ss38346943	28	C10458639T	Intron
ss38346949		A10448217G	Intron
rs1217413	35	C10443865T	Intron
ss38346948		A10443204T	UTR 3
rs1217411		C10442240T	TFBS

SNP numbers listed in table 1.

Positions are according to genomic contig NT_019273. The minor allele is listed first, followed by the position and then the major allele. The alleles are oriented according to transcript NM_012411, which is the reverse complement of the genomic contig sequence.