List of variants in gene IMPDH1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000883.4(IMPDH1):c.1108G>A (p.Ala370Thr)	rs72624961	0.00179
NM_000883.4(IMPDH1):c.402+57G>A	rs72624951	0.00169
NM_000883.4(IMPDH1):c.1598A>G (p.Gln533Arg)	rs144498273	0.00088
NM_000883.4(IMPDH1):c.189A>G (p.Ser63=)	rs143796089	0.00063
NM_000883.4(IMPDH1):c.754G>T (p.Ala252Ser)	rs756851981	0.00015
NM_000883.4(IMPDH1):c.377T>C (p.Phe126Ser)	rs367549284	0.00012

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