Table 2.

Associated SNPs to disordered eating in Mexican population.

SNP	Band	Position	A1/A2	MAF Cases	MAF Controls	OR	L95	U95	p-Value	Gene	Effect
rs17030129	1p36.31	1:7059150	A/G	0.3787	0.3145	1.685	1.325	2.141	2.03 × 10−5	CAMTA1	Intron
rs11120813		1:7062993	A/G	0.4414	0.3720	1.646	1.306	2.075	2.45 × 10−5
rs6690584		1:7078434	G/T	0.4401	0.3645	1.718	1.359	2.170	5.87 × 10−5
rs7521204	1p36.13	1:19138295	T/C	0.5329	0.4193	1.672	1.330	2.100	1.03 × 10−5	Intergenic	-
rs12024738	1q31.1	1:190694813	A/G	0.5285	0.4238	1.577	1.267	1.964	4.65 × 10−5	LINC01720	Intron
rs4626924	1q42.3	1:234909298	C/T	0.2260	0.2862	0.5861	0.4536	0.7573	4.38 × 10−5	LOC107985364
rs867286	2p21	2:45982030	A/G	0.4505	0.3821	1.655	1.321	2.074	1.18 × 10−5	PRKCE	Intron
rs11677196	2p12	2:75830221	A/G	0.2949	0.3754	0.5947	0.4688	0.7546	1.83 × 10−5	Intergenic	-
rs3205060	2q31.1	2:175425346	G/A	0.4249	0.3410	1.657	1.318	2.084	1.57 × 10−5	WIPF1	3′-UTR
rs7569439	2q35	2:220590633	C/T	0.3091	0.3712	0.57	0.4472	0.7266	5.67 × 10−6	Intergenic	-
rs35542515		4:161798045	A/C	0.2733	0.2063	1.93	1.472	2.529	1.91 × 10−6
rs2748991	6p12.2	6:52596516	C/T	0.4234	0.3099	1.662	1.303	2.118	4.16 × 10−5
rs3801220	7p14.1	7:42247876	G/A	0.5494	0.4506	1.729	1.379	2.167	2.11 × 10−6	GLI3	Intron
rs3801232		7:42253313	T/C	0.5284	0.4282	1.778	1.412	2.238	9.70 × 10−7
rs4724100		7:42264679	C/T	0.5254	0.4316	1.726	1.371	2.174	3.50 × 10−6
rs4507768	8q13.3	8:70642018	A/G	0.1272	0.1703	0.5027	0.3635	0.6952	3.23 × 10−5	SLCO5A1	Intron
rs10114881	9q21.13	9:76676071	T/C	0.5254	0.4298	1.628	1.293	2.049	3.34 × 10−5	Intergenic	-
rs12241514	10p12.31	10:21602923	A/G	0.1257	0.2088	0.4525	0.3293	0.6219	1.02 × 10−6
rs1865020	10q22.3	10:78688976	C/T	0.4566	0.3764	1.634	1.301	2.052	2.45 × 10−5	KCNMA1	Intron
rs7918074	10q26.3	10:134277154	A/G	0.2380	0.1547	1.922	1.448	2.551	6.20 × 10−6	LOC105378569
rs10870311		10:134290526	A/C	0.3228	0.2279	1.751	1.347	2.275	2.77 × 10−5	Intergenic	-
rs10772471	12p13.2	12:11600364	A/G	0.3802	0.2754	1.66	1.301	2.117	4.58 × 10−5	LOC440084	Intron
rs7297606	12q24.3	12:119568596	A/G	0.1886	0.1605	1.918	1.415	2.599	2.66 × 10−5	SRRM4	Missense (p.Ser243Asn)
rs4075945		12:119569784	T/C	0.1886	0.1609	1.915	1.413	2.599	2.78 × 10−5		Intron
rs12809631		12:131045190	A/C	0.1467	0.1954	0.5341	0.3992	0.7146	2.41 × 10−5	RIMBP2
rs2144067	14q32.31	14:101952406	T/C	0.2156	0.2330	0.5547	0.4198	0.7330	3.42 × 10−5	Intergenic	-
rs1007904		14:101955905	A/G	0.2380	0.2589	0.5720	0.4370	0.7488	4.80 × 10−5
rs7163468	15q12	15:26587077	T/C	0.2036	0.1243	1.915	1.399	2.621	4.96 × 10−5
rs3922665		15:26590830	G/A	0.2425	0.1552	1.885	1.413	2.514	1.60 × 10−5
rs8041059	15q21.3	15:58743709	T/C	0.2710	0.1999	1.732	1.329	2.256	4.72 × 10−5	LIPC	Intron
rs11073665	15q25.3	15:87295120	G/A	0.4027	0.3281	1.626	1.295	2.041	2.78 × 10−5	AGBL1
rs17135764	16p13.3	16:2111779	T/C	0.2440	0.3144	0.5455	0.4249	0.7003	1.99 × 10−6	TSC2	Intron
rs11862729	16p13.12	16:14146098	G/A	0.2395	0.1789	1.809	1.364	2.4000	3.87 × 10−5	Intergenic	-
rs12454763	18q12.3	18:42434615	A/G	0.4102	0.3341	1.673	1.328	2.108	1.26 × 10−5	SETBP1	Intron
rs991014		18:42439886	A/G	0.4096	0.3349	1.705	1.350	2.154	7.49 × 10−6
rs1042122	19q13.3	19:49989424	C/T	0.2769	0.3567	0.5677	0.4447	0.7246	5.46 × 10−6	FLT3LG	Missense (p.Phe177Leu)
rs10419198		19:50038017	T/C	0.3084	0.3833	0.6054	0.4798	0.7638	4.85 × 10−5	RCN3	Intron
rs6074170	20p12.2	20:10671078	A/G	0.4162	0.3501	1.5940	1.2730	1.9970	4.85 × 10−5	Intergenic	-
rs4813048		20:11169603	T/C	0.2575	0.1821	1.8440	1.3870	2.4520	2.55 × 10−5
rs6043684	20p12.1	20:16023836	A/C	0.4096	0.3066	1.6330	1.2980	2.0560	2.88 × 10−5	MACROD2	Intron
rs6104082	20q13.12	20:43897362	C/T	0.3423	0.2827	1.6750	1.3060	2.1470	4.70 × 10−5	LOC105372630
rs2824006	21q21.1	21:18099779	C/T	0.4386	0.3584	1.5930	1.2760	1.9900	4.00 × 10−5	Intergenic	-
rs2824065		21:18187408	C/T	0.3997	0.2968	1.6910	1.3380	2.1370	1.09 × 105
rs71330155		21:22059184	A/C	0.1587	0.2234	0.5276	0.3922	0.7098	2.38 × 10−5

Note: SNP = single-nucleotide polymorphism, Band = cytogeneitc band, Position = genomic coordinates, A1/A2 = minor allele/major allele frequency, MAF = minor allele frequency, OR = odds ratio, L95 = low 95% confidence interval, U95 = upper 95% confidence interval, Effect = in-silico variant effect prediction.