ClinVar Miner

List of variants in gene NR2F1 reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 46
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HGVS dbSNP gnomAD frequency
NM_005654.6(NR2F1):c.-187G>A rs866080178 0.02747
NM_005654.6(NR2F1):c.-1588T>C rs76981368 0.01884
NM_005654.6(NR2F1):c.463+99C>G rs533917207 0.00374
NM_005654.6(NR2F1):c.-33C>T rs372818347 0.00098
NM_005654.6(NR2F1):c.708C>T (p.Asn236=) rs372227484 0.00020
NM_005654.6(NR2F1):c.903C>A (p.Ile301=) rs750683610 0.00015
NM_005654.6(NR2F1):c.1008G>A (p.Ser336=) rs145104274 0.00005
NM_005654.6(NR2F1):c.505G>A (p.Gly169Ser) rs370606773 0.00005
NM_005654.6(NR2F1):c.1014G>A (p.Ala338=) rs201229023 0.00004
NM_005654.6(NR2F1):c.48C>T (p.Ala16=) rs780151168 0.00004
NM_005654.6(NR2F1):c.756A>G (p.Leu252=) rs547985564 0.00004
NM_005654.6(NR2F1):c.1149C>T (p.Ser383=) rs144876856 0.00003
NM_005654.6(NR2F1):c.183C>T (p.Pro61=) rs1054029785 0.00003
NM_005654.6(NR2F1):c.531C>T (p.Asp177=) rs964131641 0.00003
NM_005654.6(NR2F1):c.558C>T (p.Ser186=) rs773102110 0.00003
NM_005654.6(NR2F1):c.1023C>T (p.Ile341=) rs776732958 0.00002
NM_005654.6(NR2F1):c.540C>T (p.Asn180=) rs747863258 0.00002
NM_005654.6(NR2F1):c.1248T>A (p.Pro416=) rs753642534 0.00001
NM_005654.6(NR2F1):c.153G>A (p.Thr51=) rs1057522243 0.00001
NM_005654.6(NR2F1):c.20G>A (p.Ser7Asn) rs1753203799 0.00001
NM_005654.6(NR2F1):c.276G>A (p.Lys92=) rs906581747 0.00001
NM_005654.6(NR2F1):c.463+5A>G rs747394434 0.00001
NM_005654.6(NR2F1):c.666G>A (p.Leu222=) rs764266826 0.00001
NM_005654.6(NR2F1):c.939C>T (p.His313=) rs1018466118 0.00001
NM_005654.6(NR2F1):c.987G>A (p.Thr329=) rs757861079 0.00001
NM_005654.6(NR2F1):c.991+19G>A rs781016741 0.00001
NM_005654.6(NR2F1):c.-1751CT[11] rs140194624
NM_005654.6(NR2F1):c.-1761A>G
NM_005654.6(NR2F1):c.1044G>A (p.Ser348=) rs142689077
NM_005654.6(NR2F1):c.107_115dup (p.Gly36_Gly38dup) rs1414612574
NM_005654.6(NR2F1):c.110_115dup (p.Ala37_Gly38dup) rs1159055932
NM_005654.6(NR2F1):c.111C>G (p.Ala37=) rs1183108440
NM_005654.6(NR2F1):c.1134C>A (p.Arg378=) rs755004144
NM_005654.6(NR2F1):c.162C>T (p.Thr54=) rs557800691
NM_005654.6(NR2F1):c.165G>C (p.Pro55=) rs772383390
NM_005654.6(NR2F1):c.189C>T (p.Thr63=) rs1753208796
NM_005654.6(NR2F1):c.464-11_464-8del rs769788437
NM_005654.6(NR2F1):c.601T>A (p.Ser201Thr) rs368008985
NM_005654.6(NR2F1):c.60C>G (p.Pro20=) rs753932507
NM_005654.6(NR2F1):c.66C>T (p.Gly22=) rs971963375
NM_005654.6(NR2F1):c.72C>A (p.Asn24Lys) rs1753205307
NM_005654.6(NR2F1):c.801C>T (p.Cys267=) rs1331078890
NM_005654.6(NR2F1):c.92GCG[7] (p.Gly36dup) rs954495672
NM_005654.6(NR2F1):c.991+10C>A rs1554074872
NM_005654.6(NR2F1):c.991+12del rs774050994
NM_005654.6(NR2F1):c.992-16G>A rs946631304

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