List of variants in gene ACADVL reported as likely benign by Counsyl

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: 43

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HGVS	dbSNP	gnomAD frequency
NM_000018.4(ACADVL):c.1752-36G>A	rs200709964	0.00166
NM_000018.4(ACADVL):c.752+24C>T	rs201030339	0.00166
NM_000018.4(ACADVL):c.1606-22C>T	rs370303265	0.00139
NM_000018.4(ACADVL):c.343-41C>A	rs368107662	0.00029
NM_000018.4(ACADVL):c.1678+15C>T	rs371402802	0.00027
NM_000018.4(ACADVL):c.1751+18G>A	rs528002997	0.00026
NM_000018.4(ACADVL):c.1605+22A>G	rs1052646012	0.00014
NM_000018.4(ACADVL):c.342+25C>T	rs771711857	0.00013
NM_000018.4(ACADVL):c.1678+39C>G	rs377062362	0.00010
NM_000018.4(ACADVL):c.277+24T>C	rs199945418	0.00010
NM_000018.4(ACADVL):c.62+9G>A	rs369512281	0.00010
NM_000018.4(ACADVL):c.1751+46C>G	rs375203448	0.00009
NM_000018.4(ACADVL):c.1752-23T>C	rs368009800	0.00004
NM_000018.4(ACADVL):c.278-39C>T	rs202244937	0.00004
NM_000018.4(ACADVL):c.342+15G>A	rs777751102	0.00004
NM_000018.4(ACADVL):c.1332+27C>T	rs200161683	0.00003
NM_000018.4(ACADVL):c.1434+23G>A	rs759991740	0.00003
NM_000018.4(ACADVL):c.1532+11G>A	rs372900326	0.00003
NM_000018.4(ACADVL):c.1532+7T>C	rs534469222	0.00003
NM_000018.4(ACADVL):c.1679-34C>T	rs779439503	0.00003
NM_000018.4(ACADVL):c.1678+22C>T	rs761650394	0.00002
NM_000018.4(ACADVL):c.1678+24G>A	rs751665756	0.00002
NM_000018.4(ACADVL):c.1752-32_1752-31del	rs758750087	0.00002
NM_000018.4(ACADVL):c.342+14C>T	rs567468883	0.00002
NM_000018.4(ACADVL):c.1434+38G>C	rs763704056	0.00001
NM_000018.4(ACADVL):c.1751+30C>T	rs757837505	0.00001
NM_000018.4(ACADVL):c.1752-33C>T	rs760851448	0.00001
NM_000018.4(ACADVL):c.204+15G>A	rs1404625751	0.00001
NM_000018.4(ACADVL):c.342+16G>C	rs536497611	0.00001
NM_000018.4(ACADVL):c.343-23G>A	rs781064781	0.00001
NM_000018.4(ACADVL):c.62+10del	rs1251002707	0.00001
NM_000018.4(ACADVL):c.1270-38A>G	rs1555528742
NM_000018.4(ACADVL):c.1333-25T>C	rs770876053
NM_000018.4(ACADVL):c.1434+14T>A	rs202217537
NM_000018.4(ACADVL):c.1434+24G>A	rs1555528806
NM_000018.4(ACADVL):c.1434+27G>A	rs1271483942
NM_000018.4(ACADVL):c.1606-28G>A	rs773931227
NM_000018.4(ACADVL):c.1606-36G>A	rs890862631
NM_000018.4(ACADVL):c.1606-42C>G	rs372357967
NM_000018.4(ACADVL):c.1606-42C>T	rs372357967
NM_000018.4(ACADVL):c.1678+27C>A	rs759729168
NM_000018.4(ACADVL):c.204+31dup	rs1555527700
NM_000018.4(ACADVL):c.277+27del	rs775298132

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