List of variants in gene ADAMTSL4 reported by Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_019032.6(ADAMTSL4):c.2087C>T (p.Ser696Leu)	rs115937511	0.00142
NM_019032.6(ADAMTSL4):c.2944-7G>A	rs193025475	0.00111
NM_019032.6(ADAMTSL4):c.2559+9G>A	rs12049100	0.00033
NM_019032.6(ADAMTSL4):c.2560-4G>A	rs374389962	0.00030
NM_019032.6(ADAMTSL4):c.1483G>A (p.Gly495Arg)	rs139551885	0.00024
NM_019032.6(ADAMTSL4):c.2341C>T (p.Arg781Cys)	rs149442347	0.00012
NM_019032.6(ADAMTSL4):c.1234+90G>A	rs762772611	0.00008
NM_019032.6(ADAMTSL4):c.2839G>A (p.Val947Met)	rs145015450	0.00007
NM_019032.6(ADAMTSL4):c.1378G>A (p.Gly460Ser)	rs587749107	0.00003
NM_019032.6(ADAMTSL4):c.2008C>T (p.Arg670Ter)	rs368482584	0.00002
NM_019032.6(ADAMTSL4):c.1234+3G>A	rs1318676781	0.00001
NM_019032.6(ADAMTSL4):c.2178-10G>T	rs766540875
NM_019032.6(ADAMTSL4):c.2442T>G (p.Asn814Lys)	rs10888382
NM_019032.6(ADAMTSL4):c.767_786del (p.Gln256fs)	rs199473693
NM_019032.6(ADAMTSL4):c.963_964insT (p.Thr322fs)	rs2101584597

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