List of variants reported as likely benign for 46,XY partial gonadal dysgenesis by Fulgent Genetics, Fulgent Genetics

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_012082.4(ZFPM2):c.40+12C>G	rs149902904	0.00711
NM_000475.5(NR0B1):c.1029G>A (p.Leu343=)	rs112775648	0.00406
NM_001308093.3(GATA4):c.1235C>T (p.Ala412Val)	rs55633527	0.00326
NM_000475.5(NR0B1):c.1410A>G (p.Ile470Met)	rs151317312	0.00084
NM_012082.4(ZFPM2):c.2963A>C (p.Lys988Thr)	rs139881948	0.00073
NM_000475.5(NR0B1):c.600C>G (p.Cys200Trp)	rs143141578	0.00039
NM_005921.2(MAP3K1):c.2431A>G (p.Met811Val)	rs189290632	0.00026
NM_000475.5(NR0B1):c.469C>T (p.His157Tyr)	rs776059398	0.00009
NM_000475.5(NR0B1):c.993C>T (p.Asn331=)	rs767263700	0.00004
NM_000475.5(NR0B1):c.1176G>A (p.Pro392=)	rs778616722	0.00003
NM_005921.2(MAP3K1):c.835-11dup	rs201780112

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