MT1H[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3296502	NM_005951.2(MT1H):c.8C>T (p.Pro3Leu)	MT1H (P3L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320634	NM_005951.2(MT1H):c.40G>A (p.Ala14Thr)	MT1H (A14T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3212989	NM_005951.2(MT1H):c.50G>T (p.Gly17Val)	MT1H (G17V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241850	NM_005951.2(MT1H):c.86G>T (p.Cys29Phe)	MT1H (C29F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254180	NM_005951.2(MT1H):c.107G>A (p.Cys36Tyr)	MT1H (C36Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495368	NM_005951.2(MT1H):c.118G>C (p.Gly40Arg)	MT1H (G40R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376418	NM_005951.2(MT1H):c.157G>A (p.Ala53Thr)	MT1H (A53T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar