List of variants in gene NR2F2 studied for Inborn genetic diseases

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_021005.4(NR2F2):c.202A>G (p.Ser68Gly)	rs766186920	0.00002
NM_021005.4(NR2F2):c.95C>G (p.Pro32Arg)	rs1360897061	0.00002
NM_021005.4(NR2F2):c.100C>T (p.Pro34Ser)	rs1899167460
NM_021005.4(NR2F2):c.103G>A (p.Gly35Ser)
NM_021005.4(NR2F2):c.1097G>C (p.Arg366Pro)	rs1555447465
NM_021005.4(NR2F2):c.130G>A (p.Gly44Ser)
NM_021005.4(NR2F2):c.146C>A (p.Ala49Asp)	rs2141166777
NM_021005.4(NR2F2):c.162G>C (p.Gln54His)	rs1596424745
NM_021005.4(NR2F2):c.180G>C (p.Gln60His)
NM_021005.4(NR2F2):c.334A>G (p.Ser112Gly)	rs2505770104
NM_021005.4(NR2F2):c.649G>A (p.Ala217Thr)
NM_021005.4(NR2F2):c.64C>T (p.Gln22Ter)	rs1555446980
NM_021005.4(NR2F2):c.657G>T (p.Met219Ile)	rs774311305
NM_021005.4(NR2F2):c.696C>A (p.Phe232Leu)
NM_021005.4(NR2F2):c.76G>C (p.Ala26Pro)	rs1341003670
NM_021005.4(NR2F2):c.775C>T (p.Gln259Ter)	rs2505774793
NM_021005.4(NR2F2):c.830C>T (p.Ala277Val)
NM_021005.4(NR2F2):c.893A>G (p.Gln298Arg)
NM_021005.4(NR2F2):c.940T>C (p.Cys314Arg)	rs1555447237

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