Table 3 Allele frequencies of variants across multiple large genetic projects.

Trait	CHR	Position	SNP ID	Alt	Case	Control	TPMI^a	Twbank^b	1000g^c				gnomAD^d
Trait	CHR	Position	SNP ID	Alt	Case	Control	TPMI^a	Twbank^b	AFR	AMR	EAS	EUR	AFR	AMR	EAS	FIN	NFE
LN	7	81,805,617	rs1025129	C	0.188	0.070	0.069	0.071	0.010	0.094	0.054	0.210	0.038	0.097	0.066	0.187	0.198
	6	89,981,124	rs80282109	T	0.297	0.139	0.140	0.158	0.045	0.190	0.140	0.005	0.042	0.202	0.145	0.052	0.004
	13	112,014,681	rs516119	G	0.262	0.480	0.478	0.447	0.990	0.780	0.460	0.680	0.946	0.769	0.461	0.628	0.709
SLE	7	74,711,703	rs117026326	T	0.197	0.114	0.119	0.128	0.001	0.004	0.073	0.016	0.002	0.002	0.125	0.043	0.019
	4	188,062,888	rs12508616	A	0.162	0.095	0.097	0.086
	8	10,039,579	rs76267797	G	0.118	0.062	0.063	0.068			0.056		0.000	0.000	0.059	0.000	0.000
	7	74,619,286	rs73366469	C	0.226	0.146	0.152	0.158	0.170	0.058	0.110	0.087	0.172	0.069	0.150	0.066	0.097
LN/SLE	22	28,403,092	rs134545	C	0.492	0.260	0.293	0.298	0.580	0.390	0.290	0.380	0.553	0.295	0.279	0.328	0.344

^aTaiwan Precision Medicine Initiative.
^bTaiwan Biobank.
^c1000 Genomes global minor allele frequency.
^dgnomAD (genomes) allele frequencies.
^eAFR, African; AMR, American; EAS, East Asian; EUR, European; FIN, Finnish; NFE, Non-Finnish European; SAS, South Asian.

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