List of variants in gene AR reported as uncertain significance for Androgen resistance syndrome

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

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000044.6(AR):c.1424C>T (p.Ala475Val)	rs200390780	0.00110
NM_000044.6(AR):c.1153G>T (p.Ala385Ser)	rs200067740	0.00018
NM_000044.6(AR):c.1513C>A (p.Pro505Thr)	rs764238988	0.00002
NM_000044.6(AR):c.1370GCG[20] (p.Gly471_Gly473dup)	rs746853821
NM_000044.6(AR):c.1370GCG[5] (p.Gly462_Gly473del)	rs746853821
NM_000044.6(AR):c.1370GCG[7] (p.Gly464_Gly473del)	rs746853821
NM_000044.6(AR):c.1693G>C (p.Asp565His)
NM_000044.6(AR):c.1793G>T (p.Ser598Ile)
NM_000044.6(AR):c.1814A>G (p.Asp605Gly)	rs1555990478
NM_000044.6(AR):c.2227A>G (p.Met743Val)	rs2147530802
NM_000044.6(AR):c.2309T>G (p.Val770Gly)	rs1555996870
NM_000044.6(AR):c.2512G>A (p.Glu838Lys)	rs1555997775
NM_000044.6(AR):c.2633C>T (p.Thr878Ile)	rs137852580
NM_000044.6(AR):c.2726C>T (p.Ser909Phe)	rs2147540747
NM_000044.6(AR):c.847C>T (p.Pro283Ser)	rs1929708922
NM_000044.6(AR):c.882G>T (p.Leu294=)

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