List of variants in gene ABHD5 reported as benign for not provided

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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_016006.6(ABHD5):c.506+329C>T	rs17075884	0.08101
NM_016006.6(ABHD5):c.134-197C>A	rs9862268	0.07517
NM_016006.6(ABHD5):c.*38T>G	rs887472	0.06058
NM_016006.6(ABHD5):c.*281C>A	rs34226283	0.04705
NM_016006.6(ABHD5):c.341G>T (p.Arg114Leu)	rs148743497	0.00793
NM_016006.6(ABHD5):c.202T>C (p.Phe68Leu)	rs115209685	0.00474
NM_016006.6(ABHD5):c.961-15C>T	rs375012502	0.00038
NM_016006.6(ABHD5):c.*1860del	rs571429944
NM_016006.6(ABHD5):c.506+289TTA[2]	rs142265880
NM_016006.6(ABHD5):c.66T>C (p.Gly22=)
NM_016006.6(ABHD5):c.726C>T (p.Asp242=)
NM_016006.6(ABHD5):c.773+28TG[15]	rs10662733
NM_016006.6(ABHD5):c.773+28TG[18]	rs10662733
NM_016006.6(ABHD5):c.773+28TG[19]	rs10662733
NM_016006.6(ABHD5):c.773+28TG[20]	rs10662733
NM_016006.6(ABHD5):c.773+61_773+62insGT	rs2149604791
NM_016006.6(ABHD5):c.773+95TATT[4]	rs10544015

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