Table 1.

Identified SNPs in male (rows 1-10) and female (rows 11-18) cohorts.

SNP ID	Chromosome	Position	Gene	Mutation	Protein sequence change	Minor allele frequency	P-value	FDR BH
-	14	105,168,369	JAG2	3-base insertion	-	0.04259	7.36E−08	1.17E−02
rs17119420	12	52,810,740	KRT4	Intron variant	-	0.04748	1.66E−06	1.32E−01
rs1199015110	9	39,358,958	SPATA31A1	Missense (T > G)	Leucine to arginine	0.02691	2.84E−06	1.40E−01
rs59439901	12	52,839,305	KRT78	Silent (G > A)	-	0.04156	3.79E−06	1.40E−01
rs73106425	12	52,846,331	KRT78	Intron variant	-	0.04054	5.08E−06	1.40E−01
rs73102423	12	52,823,166	KRT79	Missense (T > C)	Lysine to arginine	0.04536	6.04E−06	1.40E−01
rs767754397	12	98,723,142	APAF1	Intron variant	-	0.01737	7.21E−06	1.40E−01
rs73106411	12	52,831,664	KRT79	Intron variant	-	0.0442	8.04E−06	1.40E−01
rs75980785	14	105,148,684	JAG2	Intron variant	-	0.03963	8.38E−06	1.40E−01
rs1287648533	10	45,953,507	PARGP1	Intron variant	-	0.01256	8.79E−06	1.40E−01
rs61734468	2	63,174,685	WDPCP	Missense (T > C)	Asparagine to serine	0.01345	3.96E−10	7.30E−05
rs74582253	17	3,882,324	CAMKK1	Missense (G > A)	Isoleucine to methionine	0.01425	2.07E−06	6.47E−03
rs78858847	2	62,859,388	EHBP1	Intron variant	-	0.01111	2.47E−06	1.12E−01
rs5610368	17	3,883,929	CAMKK1	Silent (G > A)	-	0.01257	3.05E−06	1.12E−01
rs577015585	19	51,104,412	CTU1	Missense (A > G)	Valine to alanine	0.01569	3.95E−06	1.12E−01
rs190902899	6	21,594,474	SOX4	5 prime UTR variant	-	0.01336	4.27E−06	1.12E−01
rs13058731	22	38,085,636	BAIAP2L2	Intron variant	-	0.01956	6.75E−06	1.50E−01
rs143853626	12	26,071,504	RASSF8	Intron variant	-	0.01775	7.31E−06	1.50E−01