List of variants in gene ZNF581 reported as uncertain significance by Ambry Genetics

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: 24

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HGVS	dbSNP	gnomAD frequency
NM_016535.4(ZNF581):c.149C>T (p.Pro50Leu)	rs147150085	0.00035
NM_016535.4(ZNF581):c.443C>T (p.Pro148Leu)	rs149813172	0.00006
NM_016535.4(ZNF581):c.470C>T (p.Ala157Val)	rs368531496	0.00005
NM_016535.4(ZNF581):c.494G>A (p.Arg165Gln)	rs755855678	0.00003
NM_016535.4(ZNF581):c.68C>T (p.Pro23Leu)	rs112877603	0.00003
NM_016535.4(ZNF581):c.377G>A (p.Arg126His)	rs1203196285	0.00001
NM_016535.4(ZNF581):c.394C>T (p.Arg132Trp)	rs963978113	0.00001
NM_016535.4(ZNF581):c.406A>G (p.Ile136Val)	rs762357518	0.00001
NM_016535.4(ZNF581):c.454C>T (p.Arg152Cys)	rs1417390736	0.00001
NM_016535.4(ZNF581):c.73C>T (p.Arg25Cys)	rs1165235660	0.00001
NM_016535.4(ZNF581):c.74G>A (p.Arg25His)	rs376022915	0.00001
NM_016535.4(ZNF581):c.110C>G (p.Ser37Cys)	rs1380720012
NM_016535.4(ZNF581):c.131C>T (p.Ala44Val)
NM_016535.4(ZNF581):c.139C>T (p.Pro47Ser)	rs1982747766
NM_016535.4(ZNF581):c.297G>A (p.Met99Ile)	rs1459939022
NM_016535.4(ZNF581):c.346G>A (p.Glu116Lys)
NM_016535.4(ZNF581):c.379G>T (p.Ala127Ser)
NM_016535.4(ZNF581):c.452C>T (p.Pro151Leu)
NM_016535.4(ZNF581):c.457C>T (p.Arg153Cys)
NM_016535.4(ZNF581):c.511C>A (p.Arg171Ser)	rs201594382
NM_016535.4(ZNF581):c.514C>T (p.Pro172Ser)	rs2514172970
NM_016535.4(ZNF581):c.538C>T (p.Arg180Cys)	rs778131710
NM_016535.4(ZNF581):c.578G>A (p.Arg193Gln)
NM_016535.4(ZNF581):c.70C>T (p.Pro24Ser)	rs12982230

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