List of variants in gene combination AR, LOC109504725 reported as benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000044.6(AR):c.171GCA[18] (p.Gln76_Gln80del)	rs3032358
NM_000044.6(AR):c.171GCA[19] (p.Gln77_Gln80del)	rs3032358
NM_000044.6(AR):c.171GCA[20] (p.Gln78_Gln80del)	rs3032358
NM_000044.6(AR):c.171GCA[21] (p.Gln79_Gln80del)	rs3032358
NM_000044.6(AR):c.171GCA[22] (p.Gln80del)	rs3032358
NM_000044.6(AR):c.171GCA[24] (p.Gln80dup)	rs3032358
NM_000044.6(AR):c.171GCA[25] (p.Gln79_Gln80dup)	rs3032358
NM_000044.6(AR):c.171GCA[26] (p.Gln78_Gln80dup)	rs3032358
NM_000044.6(AR):c.171GCA[27] (p.Gln77_Gln80dup)	rs3032358
NM_000044.6(AR):c.171GCA[28] (p.Gln76_Gln80dup)	rs3032358
NM_000044.6(AR):c.231_232insGCAGCAGCA (p.Gln77_Gln78insAlaAlaAla)	rs4045402

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