List of variants in gene IMPDH1 reported as likely pathogenic 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000883.4(IMPDH1):c.255-2A>G	rs1238921380	0.00002
NC_000007.14:g.(?_128392911)_(128393755_?)del
NM_000883.4(IMPDH1):c.1262-1G>T
NM_000883.4(IMPDH1):c.1405+1G>A
NM_000883.4(IMPDH1):c.936GAA[2] (p.Lys314del)	rs1554414710
NM_000883.4(IMPDH1):c.968A>G (p.Lys323Arg)	rs1798086782

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