List of variants in gene POMGNT2 reported as likely benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_032806.6(POMGNT2):c.674G>A (p.Arg225Gln)	rs138980930	0.00208
NM_032806.6(POMGNT2):c.966C>G (p.Ser322=)	rs141319921	0.00186
NM_032806.6(POMGNT2):c.1388G>A (p.Arg463His)	rs143394182	0.00081
NM_032806.6(POMGNT2):c.488A>G (p.Asn163Ser)	rs140389725	0.00067
NM_032806.6(POMGNT2):c.1602C>T (p.Tyr534=)	rs143832191	0.00066
NM_032806.6(POMGNT2):c.561C>T (p.His187=)	rs147429438	0.00059
NM_032806.6(POMGNT2):c.438G>A (p.Pro146=)	rs375314883	0.00036
NM_032806.6(POMGNT2):c.454G>A (p.Val152Met)	rs201114442	0.00011
NM_032806.6(POMGNT2):c.1137G>A (p.Thr379=)	rs377724350	0.00010
NM_032806.6(POMGNT2):c.459C>T (p.Ala153=)	rs373276653	0.00005
NM_032806.6(POMGNT2):c.1181G>A (p.Arg394Gln)	rs199612856	0.00004
NM_032806.6(POMGNT2):c.81G>A (p.Glu27=)	rs201572917	0.00003
NM_032806.6(POMGNT2):c.264C>T (p.Asn88=)	rs572228301	0.00001
NM_032806.6(POMGNT2):c.39G>C (p.Ser13=)	rs59831271
NM_032806.6(POMGNT2):c.444C>T (p.Phe148=)

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