List of variants in gene ENTPD1 reported as uncertain significance 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_001776.6(ENTPD1):c.424G>C (p.Glu142Gln)	rs148809600	0.00017
NM_001776.6(ENTPD1):c.1220A>G (p.Lys407Arg)
NM_001776.6(ENTPD1):c.1478T>C (p.Ile493Thr)
NM_001776.6(ENTPD1):c.706G>T (p.Ala236Ser)
NM_001776.6(ENTPD1):c.780G>C (p.Gln260His)	rs1555303223
NM_001776.6(ENTPD1):c.896C>T (p.Thr299Ile)

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