List of variants in gene LOC126807392, MAP3K1 studied for 46,XY sex reversal 6

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_005921.2(MAP3K1):c.3190A>C (p.Arg1064=)	rs832583	0.77675
NM_005921.2(MAP3K1):c.3667-13G>A	rs16886463	0.08897
NM_005921.2(MAP3K1):c.3588A>C (p.Ser1196=)	rs55912465	0.00337
NM_005921.2(MAP3K1):c.3498C>T (p.Thr1166=)	rs200078723	0.00010
NM_005921.2(MAP3K1):c.3242T>A (p.Met1081Lys)	rs754640057	0.00005
NM_005921.2(MAP3K1):c.3275A>G (p.Asp1092Gly)	rs374418331	0.00005
NM_005921.2(MAP3K1):c.3667-4G>T	rs552563402	0.00005
NM_005921.2(MAP3K1):c.3667-7T>C	rs117348142	0.00004
NM_005921.2(MAP3K1):c.3266C>G (p.Ser1089Cys)	rs755658722	0.00003
NM_005921.2(MAP3K1):c.3416C>T (p.Ser1139Phe)	rs750141197	0.00001
NM_005921.2(MAP3K1):c.3198C>G (p.Thr1066=)	rs918712593
NM_005921.2(MAP3K1):c.3212G>T (p.Ser1071Ile)	rs748409131
NM_005921.2(MAP3K1):c.3263G>C (p.Ser1088Thr)
NM_005921.2(MAP3K1):c.3334G>A (p.Val1112Met)
NM_005921.2(MAP3K1):c.3608C>G (p.Pro1203Arg)	rs2530958100
NM_005921.2(MAP3K1):c.3609C>T (p.Pro1203=)	rs1554035881
NM_005921.2(MAP3K1):c.3667-4G>A	rs552563402

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