ClinVar Miner

List of variants in gene NR2F2 reported as likely benign for cardiovascular disorder

Included ClinVar conditions (1426):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_021005.4(NR2F2):c.537C>T (p.Ser179=) rs143951395 0.00055
NM_021005.4(NR2F2):c.129C>G (p.Pro43=) rs551936462 0.00029
NM_021005.4(NR2F2):c.816C>G (p.Ala272=) rs76163938 0.00019
NM_021005.4(NR2F2):c.357G>C (p.Arg119=) rs137861279 0.00007
NM_021005.4(NR2F2):c.264C>G (p.Gly88=) rs757445345 0.00004
NM_021005.4(NR2F2):c.843C>T (p.Ser281=) rs1006491294 0.00003
NM_021005.4(NR2F2):c.443-5C>T rs374487006 0.00002
NM_021005.4(NR2F2):c.1206C>T (p.Ser402=) rs757077299 0.00001
NM_021005.4(NR2F2):c.789C>T (p.Pro263=) rs1174849712 0.00001
NM_021005.4(NR2F2):c.882C>T (p.Ile294=) rs1163679972 0.00001
NM_021005.4(NR2F2):c.918C>T (p.His306=) rs751816358 0.00001
NM_021005.4(NR2F2):c.971-11C>T rs1208596248 0.00001
NM_021005.4(NR2F2):c.1008C>T (p.Ser336=) rs767004289
NM_021005.4(NR2F2):c.150C>T (p.Ser50=)
NM_021005.4(NR2F2):c.210G>A (p.Lys70=) rs1899171814
NM_021005.4(NR2F2):c.237C>T (p.Cys79=)
NM_021005.4(NR2F2):c.276C>T (p.Gly92=) rs1332151769
NM_021005.4(NR2F2):c.36G>A (p.Gln12=) rs2141166624
NM_021005.4(NR2F2):c.414G>A (p.Lys138=) rs1373249033
NM_021005.4(NR2F2):c.456C>T (p.Gly152=)
NM_021005.4(NR2F2):c.468G>T (p.Pro156=) rs746596432
NM_021005.4(NR2F2):c.648C>A (p.Ala216=)
NM_021005.4(NR2F2):c.687C>T (p.Asn229=)
NM_021005.4(NR2F2):c.819C>T (p.Ala273=)
NM_021005.4(NR2F2):c.879G>A (p.Arg293=)
NM_021005.4(NR2F2):c.958C>T (p.Leu320=) rs1596428579

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