List of variants in gene combination KDM6B, LOC121587574 reported as likely benign for Inborn genetic diseases

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001348716.2(KDM6B):c.3940C>T (p.Pro1314Ser)	rs140925165
NM_001348716.2(KDM6B):c.3970C>A (p.His1324Asn)
NM_001348716.2(KDM6B):c.4259C>T (p.Thr1420Ile)	rs201258301
NM_001348716.2(KDM6B):c.4536G>T (p.Val1512=)	rs772709518

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