ClinVar Miner

List of variants reported as uncertain significance for 46,XY sex reversal 9

Included ClinVar conditions (1):
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Total variants: 19
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HGVS dbSNP
NM_012082.4(ZFPM2):c.1210A>C (p.Thr404Pro)
NM_012082.4(ZFPM2):c.1274A>T (p.Lys425Met)
NM_012082.4(ZFPM2):c.1318A>G (p.Lys440Glu)
NM_012082.4(ZFPM2):c.1436T>C (p.Leu479Pro)
NM_012082.4(ZFPM2):c.1871C>G (p.Ser624Cys) rs34248551
NM_012082.4(ZFPM2):c.1889C>T (p.Thr630Ile)
NM_012082.4(ZFPM2):c.2096A>C (p.His699Pro) rs368486644
NM_012082.4(ZFPM2):c.2146C>T (p.Pro716Ser) rs1554583195
NM_012082.4(ZFPM2):c.2206C>T (p.Arg736Cys)
NM_012082.4(ZFPM2):c.2300A>G (p.Asn767Ser)
NM_012082.4(ZFPM2):c.2384T>C (p.Val795Ala) rs1563574497
NM_012082.4(ZFPM2):c.240G>T (p.Gly80=) rs765866053
NM_012082.4(ZFPM2):c.2651G>A (p.Arg884His)
NM_012082.4(ZFPM2):c.2969G>A (p.Ser990Asn)
NM_012082.4(ZFPM2):c.3086A>T (p.Lys1029Ile) rs201729935
NM_012082.4(ZFPM2):c.3294G>C (p.Glu1098Asp) rs149688628
NM_012082.4(ZFPM2):c.3334A>G (p.Ser1112Gly) rs1554583419
NM_012082.4(ZFPM2):c.364G>T (p.Val122Leu) rs772114579
NM_012082.4(ZFPM2):c.444G>C (p.Met148Ile) rs373855468

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