List of variants in gene DNAH17 reported as benign for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 27

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HGVS	dbSNP	gnomAD frequency
NM_173628.4(DNAH17):c.11858A>G (p.His3953Arg)	rs12941494	0.95067
NM_173628.4(DNAH17):c.1770A>G (p.Lys590=)	rs894966	0.94663
NM_173628.4(DNAH17):c.5956A>G (p.Met1986Val)	rs691652	0.86865
NM_173628.4(DNAH17):c.5171G>A (p.Arg1724Lys)	rs930571	0.86857
NM_173628.4(DNAH17):c.5535T>C (p.Pro1845=)	rs2028734	0.86600
NM_173628.4(DNAH17):c.5955C>G (p.Leu1985=)	rs606944	0.86342
NM_173628.4(DNAH17):c.2547A>G (p.Leu849=)	rs7221209	0.77600
NM_173628.4(DNAH17):c.8907C>T (p.Ser2969=)	rs691225	0.66535
NM_173628.4(DNAH17):c.5226G>T (p.Met1742Ile)	rs690844	0.66261
NM_173628.4(DNAH17):c.12681C>T (p.Tyr4227=)	rs2271613	0.64491
NM_173628.4(DNAH17):c.6975T>C (p.Ile2325=)	rs691151	0.62420
NM_173628.4(DNAH17):c.3496T>C (p.Leu1166=)	rs4273108	0.61559
NM_173628.4(DNAH17):c.10449C>G (p.Thr3483=)	rs2289751	0.48833
NM_173628.4(DNAH17):c.8040C>T (p.Leu2680=)	rs7405830	0.35359
NM_173628.4(DNAH17):c.2031+11G>A	rs78321431	0.32191
NM_173628.4(DNAH17):c.1198-7C>T	rs72920970	0.30825
NM_173628.4(DNAH17):c.5904-15C>T	rs11077375	0.22557
NM_173628.4(DNAH17):c.3834A>G (p.Leu1278=)	rs17729253	0.19095
NM_173628.4(DNAH17):c.13101T>C (p.Pro4367=)	rs36119275	0.17594
NM_173628.4(DNAH17):c.13104G>A (p.Pro4368=)	rs35422926	0.17590
NM_173628.4(DNAH17):c.3659G>A (p.Arg1220His)	rs61744544	0.13251
NM_173628.4(DNAH17):c.3302C>G (p.Ala1101Gly)	rs61741523	0.12730
NM_173628.4(DNAH17):c.11857C>T (p.His3953Tyr)	rs61742072	0.12590
NM_173628.4(DNAH17):c.8505C>T (p.Asp2835=)	rs61746438	0.11258
NM_173628.4(DNAH17):c.13125C>T (p.Tyr4375=)	rs1134541	0.11233
NM_173628.4(DNAH17):c.12627G>A (p.Pro4209=)	rs3209030	0.08659
NM_173628.4(DNAH17):c.7422G>C (p.Thr2474=)	rs11872051

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