List of variants in gene HSD17B4 reported as likely benign for not specified

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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: 17

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HGVS	dbSNP	gnomAD frequency
NM_000414.4(HSD17B4):c.1210-8T>C	rs34254740	0.00123
NM_000414.4(HSD17B4):c.948A>G (p.Ala316=)	rs192301957	0.00034
NM_000414.4(HSD17B4):c.1261+14A>G	rs371682983	0.00029
NM_000414.4(HSD17B4):c.622+15T>A	rs201280286	0.00024
NM_000414.4(HSD17B4):c.264T>C (p.Asp88=)	rs763999607	0.00003
NM_000414.4(HSD17B4):c.-17C>T	rs372388554	0.00002
NM_000414.4(HSD17B4):c.58+195C>T	rs574416522	0.00002
NM_000414.4(HSD17B4):c.714+12T>G	rs762828103	0.00002
NM_000414.4(HSD17B4):c.1596T>C (p.His532=)	rs758045328	0.00001
NM_000414.4(HSD17B4):c.1875C>G (p.Thr625=)	rs745478996	0.00001
NM_000414.4(HSD17B4):c.622+14C>T	rs765736425	0.00001
NM_000414.4(HSD17B4):c.1095T>C (p.Tyr365=)	rs1554065300
NM_000414.4(HSD17B4):c.113-2248T>C	rs876657476
NM_000414.4(HSD17B4):c.1450A>G (p.Ile484Val)	rs775297352
NM_000414.4(HSD17B4):c.1471G>A (p.Ala491Thr)	rs28943591
NM_000414.4(HSD17B4):c.1809G>A (p.Val603=)	rs1279792063
NM_000414.4(HSD17B4):c.2121+7T>C	rs876657477

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