List of variants in gene AR reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000044.6(AR):c.2395C>G (p.Gln799Glu)	rs137852591	0.00137
NM_000044.6(AR):c.528C>A (p.Ser176Arg)	rs777131133	0.00024
NM_000044.6(AR):c.1368T>C (p.Gly456=)	rs866187574	0.00015
NM_000044.6(AR):c.1723C>G (p.Leu575Val)	rs376443652	0.00003
NM_000044.6(AR):c.-913C>A
NM_000044.6(AR):c.1365T>C (p.Gly455=)
NM_000044.6(AR):c.1368_1376dup (p.Gly473_Glu474insGlyGlyGly)
NM_000044.6(AR):c.1370GCG[20] (p.Gly471_Gly473dup)	rs746853821
NM_000044.6(AR):c.1377C>T (p.Gly459=)
NM_000044.6(AR):c.1769-5148A>G
NM_000044.6(AR):c.1769-5189A>T
NM_000044.6(AR):c.1769-61G>A
NM_000044.6(AR):c.2449+192C>T
NM_000044.6(AR):c.2679G>A (p.Pro893=)
NM_000044.6(AR):c.888C>T (p.Asp296=)
NM_000044.6(AR):c.957G>T (p.Gly319=)

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