List of variants in gene combination G6PC3, LOC130060959 reported as likely benign for leukopenia

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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: 33

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HGVS	dbSNP	gnomAD frequency
NM_138387.4(G6PC3):c.187A>C (p.Ile63Leu)	rs34878178	0.00124
NM_138387.4(G6PC3):c.201C>T (p.Leu67=)	rs375273894	0.00002
NM_138387.4(G6PC3):c.132C>T (p.Pro44=)	rs200427598	0.00001
NM_138387.4(G6PC3):c.105C>A (p.Pro35=)
NM_138387.4(G6PC3):c.108G>A (p.Lys36=)
NM_138387.4(G6PC3):c.129C>T (p.Phe43=)
NM_138387.4(G6PC3):c.138C>T (p.Ala46=)
NM_138387.4(G6PC3):c.141C>T (p.Tyr47=)
NM_138387.4(G6PC3):c.147C>T (p.Ala49=)
NM_138387.4(G6PC3):c.153C>G (p.Arg51=)	rs761215881
NM_138387.4(G6PC3):c.165C>T (p.Ile55=)
NM_138387.4(G6PC3):c.168G>T (p.Ala56=)
NM_138387.4(G6PC3):c.171G>A (p.Val57=)
NM_138387.4(G6PC3):c.171G>T (p.Val57=)	rs759787635
NM_138387.4(G6PC3):c.192C>T (p.Thr64=)	rs780837377
NM_138387.4(G6PC3):c.207C>G (p.Leu69=)
NM_138387.4(G6PC3):c.207C>T (p.Leu69=)
NM_138387.4(G6PC3):c.213C>T (p.Phe71=)	rs1392954032
NM_138387.4(G6PC3):c.218+14G>C
NM_138387.4(G6PC3):c.218+16C>T
NM_138387.4(G6PC3):c.218+17del
NM_138387.4(G6PC3):c.218+18T>C
NM_138387.4(G6PC3):c.218+20C>T
NM_138387.4(G6PC3):c.218+8A>G
NM_138387.4(G6PC3):c.218+9G>C
NM_138387.4(G6PC3):c.57A>G (p.Leu19=)
NM_138387.4(G6PC3):c.60C>G (p.Ala20=)
NM_138387.4(G6PC3):c.81C>G (p.Leu27=)
NM_138387.4(G6PC3):c.81C>T (p.Leu27=)	rs1324312988
NM_138387.4(G6PC3):c.87C>A (p.Ile29=)
NM_138387.4(G6PC3):c.90C>T (p.Thr30=)
NM_138387.4(G6PC3):c.99C>A (p.Gly33=)
NM_138387.4(G6PC3):c.99C>T (p.Gly33=)

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