List of variants reported as likely benign for premature ovarian failure 1

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_002024.6(FMR1):c.357A>C (p.Lys119Asn)	rs201580891	0.13140
NM_002191.4(INHA):c.769G>A (p.Ala257Thr)	rs12720062	0.01646
NM_002024.6(FMR1):c.18G>T (p.Val6=)	rs111485627	0.00830
NM_017696.3(MCM9):c.911A>G (p.Asn304Ser)	rs78231991	0.00344
NM_002024.6(FMR1):c.1572C>T (p.Ser524=)	rs143889976	0.00125

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