Mapping of a blood pressure QTL on chromosome 17 in American Indians of the strong heart family study

Table 3 Results from BQTN analyses for the panel 1 single nucleotide variants with the highest associations with systolic blood pressure

Gene	SNV	Average	SE	Posterior probability	N SNVs eligible	N SNVs *BQTN*
AZI1	rs12939525	−0.0165	0.0137	0.66	8	4
HRNBP3	rs8070973	−0.0099	0.0095	0.59	79	15
TBC1D16	rs1115834	0.0055	0.0110	0.23	12	10
TBC1D16	rs2362384	0.0290	0.0272	0.59	12	10
SLC38A10	rs7214678	−0.0146	0.0140	0.56	15	8
RNF157	rs12950642	0.0150	0.0102	0.77	20	8
RNF157	rs881502	−0.0193	0.0121	0.77	20	8
RPTOR	rs9899051	0.0098	0.0095	0.58	94	15

ISSN: 1471-2261