List of variants in gene combination LOC129993918, MAP3K1 reported as uncertain significance for 46,XY sex reversal 6

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_005921.2(MAP3K1):c.44C>G (p.Pro15Arg)	rs765282250	0.00012
NM_005921.2(MAP3K1):c.86G>A (p.Gly29Glu)	rs1581198964	0.00003
NM_005921.2(MAP3K1):c.163G>A (p.Ala55Thr)	rs769918068	0.00002
NM_005921.2(MAP3K1):c.331C>T (p.Pro111Ser)	rs1485123901	0.00001
NM_005921.2(MAP3K1):c.138G>T (p.Glu46Asp)	rs1051867310
NM_005921.2(MAP3K1):c.13G>C (p.Ala5Pro)	rs2530790408
NM_005921.2(MAP3K1):c.152G>C (p.Gly51Ala)
NM_005921.2(MAP3K1):c.161G>A (p.Arg54Gln)	rs1050828981
NM_005921.2(MAP3K1):c.170GGC[5] (p.Arg60dup)	rs746070735
NM_005921.2(MAP3K1):c.311G>A (p.Gly104Asp)	rs2111727408
NM_005921.2(MAP3K1):c.352A>T (p.Ser118Cys)
NM_005921.2(MAP3K1):c.361G>A (p.Gly121Ser)	rs779217907
NM_005921.2(MAP3K1):c.458C>T (p.Pro153Leu)	rs576080629
NM_005921.2(MAP3K1):c.5CGG[5] (p.Ala5dup)	rs779149827
NM_005921.2(MAP3K1):c.5CGG[6] (p.Ala5_Gly6insAlaAla)	rs779149827

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