ClinVar Miner

List of variants reported as benign for 46,XY sex reversal 6 by Invitae

Included ClinVar conditions (1):
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Total variants: 20
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HGVS dbSNP
NM_005921.2(MAP3K1):c.1566C>T (p.Thr522=) rs2229882
NM_005921.2(MAP3K1):c.1644A>G (p.Gln548=) rs56225368
NM_005921.2(MAP3K1):c.165G>A (p.Ala55=) rs189140884
NM_005921.2(MAP3K1):c.1917G>A (p.Leu639=) rs2229883
NM_005921.2(MAP3K1):c.233T>C (p.Leu78Pro) rs572205361
NM_005921.2(MAP3K1):c.233_234delinsCT (p.Leu78Pro) rs1554028405
NM_005921.2(MAP3K1):c.234C>T (p.Leu78=) rs542526689
NM_005921.2(MAP3K1):c.2665G>C (p.Val889Leu) rs56228802
NM_005921.2(MAP3K1):c.2816C>G (p.Ser939Cys) rs45556841
NM_005921.2(MAP3K1):c.2953_2955del (p.Thr985del) rs140733770
NM_005921.2(MAP3K1):c.3087C>T (p.Phe1029=) rs146112116
NM_005921.2(MAP3K1):c.3498C>T (p.Thr1166=) rs200078723
NM_005921.2(MAP3K1):c.3588A>C (p.Ser1196=) rs55912465
NM_005921.2(MAP3K1):c.394G>C (p.Asp132His) rs557606535
NM_005921.2(MAP3K1):c.483-18151A>G rs16886397
NM_005921.2(MAP3K1):c.710A>G (p.Gln237Arg) rs55694258
NM_005921.2(MAP3K1):c.720G>A (p.Ala240=) rs56279792
NM_005921.2(MAP3K1):c.764A>G (p.Asn255Ser) rs56069227
NM_005921.2(MAP3K1):c.81C>T (p.Gly27=) rs185050655
NM_005921.2(MAP3K1):c.834+9A>G rs73135067

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