List of variants in gene PIGG reported as likely pathogenic for syndromic intellectual disability

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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: 19

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HGVS	dbSNP	gnomAD frequency
NM_001127178.3(PIGG):c.1515G>A (p.Trp505Ter)	rs150259543	0.00073
NM_001127178.3(PIGG):c.2552A>C (p.Gln851Pro)	rs150802299	0.00014
NM_001127178.3(PIGG):c.1332+1G>A	rs779043705	0.00001
NM_001127178.3(PIGG):c.352C>T (p.Arg118Ter)	rs782124562	0.00001
NM_001127178.3(PIGG):c.498G>A (p.Trp166Ter)	rs1418085145	0.00001
NM_001127178.3(PIGG):c.1030A>C (p.Met344Leu)	rs757141700
NM_001127178.3(PIGG):c.1114+2T>G
NM_001127178.3(PIGG):c.1332+1G>T	rs779043705
NM_001127178.3(PIGG):c.1333-1G>A
NM_001127178.3(PIGG):c.154+2T>C
NM_001127178.3(PIGG):c.2069+1G>C	rs2108969826
NM_001127178.3(PIGG):c.2069+2T>G
NM_001127178.3(PIGG):c.2778_2782del (p.Cys927fs)
NM_001127178.3(PIGG):c.342dup (p.Thr115fs)	rs886041687
NM_001127178.3(PIGG):c.571del	rs1553880098
NM_001127178.3(PIGG):c.641A>G (p.His214Arg)
NM_001127178.3(PIGG):c.759+2T>C	rs1720189292
NM_001127178.3(PIGG):c.760-2A>G
NM_001127178.3(PIGG):c.768_769dup (p.Thr257fs)	rs1229339759

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