Related gene-specific medical variations for Gene (Select 474382) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3103669	NM_001017990.2(H2AB1):c.65G>A (p.Arg22His)	F8, H2AB1 +1 more (R22H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3103668	NM_001017990.2(H2AB1):c.323C>G (p.Ser108Cys)	F8, H2AB1 +1 more (S108C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3103667	NM_001017990.2(H2AB1):c.119G>A (p.Arg40Gln)	F8, H2AB1 +1 more (R40Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2608662	NM_001017990.2(H2AB1):c.56C>T (p.Thr19Ile)	F8, H2AB1 +1 more (T19I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2523862	NM_001017990.2(H2AB1):c.307A>G (p.Asn103Asp)	F8, H2AB1 +1 more (N103D)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2509933	NM_001017990.2(H2AB1):c.52C>T (p.Arg18Trp)	F8, H2AB1 +1 more (R18W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2471110	NM_001017990.2(H2AB1):c.241C>T (p.Arg81Trp)	F8, H2AB1 +1 more (R81W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1695326	NM_001017990.2(H2AB1):c.111C>T (p.Arg37=)	F8, H2AB1 +1 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign

ClinVar