List of variants in gene HSD17B10 reported as uncertain significance 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_004493.3(HSD17B10):c.13T>C (p.Cys5Arg)	rs781935025	0.00009
NM_004493.3(HSD17B10):c.349G>A (p.Val117Ile)	rs2521097701
NM_004493.3(HSD17B10):c.401G>C (p.Gly134Ala)	rs2521096231
NM_004493.3(HSD17B10):c.416A>G (p.Asn139Ser)	rs2075826960
NM_004493.3(HSD17B10):c.685G>A (p.Asp229Asn)	rs931676673

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