List of variants in gene ANKRD11 reported as likely benign for Intellectual disability

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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_013275.6(ANKRD11):c.6065C>T (p.Pro2022Leu)	rs373218212	0.00051
NM_013275.6(ANKRD11):c.3437C>T (p.Thr1146Met)	rs150325340	0.00024
NM_013275.6(ANKRD11):c.3743C>T (p.Ala1248Val)	rs752060365	0.00007
NM_013275.6(ANKRD11):c.6095C>T (p.Pro2032Leu)	rs746355740	0.00006
NM_013275.6(ANKRD11):c.3812C>T (p.Ser1271Leu)	rs767520089	0.00001
NM_013275.6(ANKRD11):c.3932G>A (p.Arg1311Gln)	rs534628110
NM_013275.6(ANKRD11):c.4022C>T (p.Pro1341Leu)	rs1456520981
NM_013275.6(ANKRD11):c.4434C>G (p.Asp1478Glu)	rs1239629602
NM_013275.6(ANKRD11):c.5160C>G (p.His1720Gln)	rs1035902808
NM_013275.6(ANKRD11):c.5323G>T (p.Ala1775Ser)	rs559618415

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