List of variants reported as benign for Premature ovarian failure 5

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Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_001080413.3(NOBOX):c.262C>T (p.Leu88=)	rs727714	0.60215
NM_001080413.3(NOBOX):c.1154+11T>C	rs757388	0.60213
NM_001080413.3(NOBOX):c.1155-23G>A	rs11769847	0.60213
NM_001080413.3(NOBOX):c.1549T>C (p.Phe517Leu)	rs2699503	0.58167
NM_001080413.3(NOBOX):c.1240+34G>A	rs11769787	0.42719
NM_001080413.3(NOBOX):c.1444G>A (p.Gly482Ser)	rs2525702	0.17402
NM_001080413.3(NOBOX):c.42T>C (p.Gly14=)	rs1208179	0.12679
NM_001080413.3(NOBOX):c.1796C>A (p.Pro599His)	rs1208216	0.12390
NM_001080413.3(NOBOX):c.1991A>G (p.Lys664Arg)	rs77802098	0.03031
NM_001080413.3(NOBOX):c.66T>C (p.Asp22=)	rs138463368	0.01148
NM_001080413.3(NOBOX):c.1354G>A (p.Asp452Asn)	rs112190116	0.00864
NM_001080413.3(NOBOX):c.1775-8C>A	rs149880524	0.00688
NM_001080413.3(NOBOX):c.131G>T (p.Arg44Leu)	rs115206969	0.00497
NM_001080413.3(NOBOX):c.86-8C>T	rs189548165	0.00481
NM_001080413.3(NOBOX):c.1856C>T (p.Pro619Leu)	rs146227301	0.00384
NM_001080413.3(NOBOX):c.454G>A (p.Gly152Arg)	rs201806397	0.00316
NM_001080413.3(NOBOX):c.293-15G>A	rs200651935	0.00298
NM_001080413.3(NOBOX):c.1709C>T (p.Ser570Leu)	rs371874278	0.00026
NM_001080413.3(NOBOX):c.68G>A (p.Gly23Asp)	rs563911669	0.00004

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