List of variants reported as likely benign for Parietal foramina 2 by Illumina Laboratory Services, Illumina

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_021926.4(ALX4):c.*290T>C	rs7128671	0.00637
NM_021926.4(ALX4):c.*2349C>A	rs139570599	0.00210
NM_021926.4(ALX4):c.*899C>T	rs543627488	0.00113
NM_021926.4(ALX4):c.*3805G>A	rs373307279	0.00108
NM_021926.4(ALX4):c.1035C>T (p.Ser345=)	rs140652481	0.00064
NM_021926.4(ALX4):c.917C>T (p.Pro306Leu)	rs149897209	0.00052
NM_021926.4(ALX4):c.1182G>A (p.Ala394=)	rs149365713	0.00031
NM_021926.4(ALX4):c.1149C>T (p.Asn383=)	rs376675326	0.00016
NM_021926.4(ALX4):c.188G>A (p.Arg63Gln)	rs372830230	0.00016
NM_021926.4(ALX4):c.728C>T (p.Ala243Val)	rs145166164	0.00013
NM_021926.4(ALX4):c.*563C>T	rs574340639	0.00011
NM_021926.4(ALX4):c.*407G>A	rs539799951	0.00009
NM_021926.4(ALX4):c.*196C>T	rs189945537	0.00005
NM_021926.4(ALX4):c.1218C>T (p.Ala406=)	rs745849255	0.00002
NM_021926.4(ALX4):c.*25C>T	rs780898515	0.00001
NM_021926.4(ALX4):c.*2861C>A	rs192487688

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