Table 3.

List of variants with (A) positive and (B) negative correlation (FDR < 0.01).

rs ID	Location	Allele	Consequence	Gene symbol	FDR (Spearman)	Captured alleles (Tagger)
A
rs3027012	1:159204333-159204333	T	5' UTR	ACKR1	0.000119	rs3027008, rs6676002
rs72717040	1:161517662-161517662	C	Intronic	FCGR2A	0.004313	rs17400517
rs7683365	4:143999443-143999443	A	Missense	GYPB	0.000161	rs7662277, rs7666297, rs7666296, rs12499907, rs12499906, rs10002395, rs10025455, rs7661933
rs17622656	5:132485305-132485305	A	Intronic	IRF1	0.002085
rs2770146	9:117711060-117711060	C	Intronic	TLR4	0.000303	rs5030728
rs2285002	14:64816958-64816958	A	Intronic	SPTB	0.005651
rs12587471	14:64825597-64825597	G	Intronic	SPTB	0.004638	rs11158561, rs4899147
rs7149121	14:64864227-64864227	C	Intronic	SPTB	0.000360
rs28370916	14:64879376-64879376	G	Intronic	SPTB	0.008414
rs8081235	17:15964787-15964787	T	Intronic	ADORA2B	0.001541
rs8081547	17:15965007-15965007	T	Intronic	ADORA2B	0.000487
B
rs6840234	4:143996657-143996657	C	intronic	GYPB	0.000468	rs6857129, rs4835127, rs1473055, rs6537238, rs4835126, rs6816184
rs8176725	9:133257230-133257230	A	intronic	ABO	0.009139
rs74056021	14:64802733-64802733	C	intronic	SPTB	0.001538	rs74056022, rs45617438
rs1535450	14:64840590-64840590	T	intronic	SPTB	0.003294	rs1475101
rs28998799	17:27799104-27799105	-	intronic	NOS2	0.000173
rs4646120	X:15599613-15599613	A	intronic	ACE2	0.006377
rs1978124	X:15599940-15599940	C	intronic	ACE2	0.001095

The first column “rsID” indicates the tag SNVs. “Location” column indicates chromosome and position in the Human Reference Genome Hg38; “Allele” column is the variant allele, “Consequence” column represents the impact of the variant (rsID) on the protein, and the “Gene symbol” is the gene where the variant is located. In “FDR (Spearman)” the FDR value for each SNVs has been reported (data from the first wave). The last column “Captured alleles (Tagger)” displays the rs number of all the SNVs in linkage disequilibrium with the tag SNV, according to Tagger analysis.