ClinVar Miner

List of variants in gene FOXP1 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_001349338.3(FOXP1):c.1889+20C>A rs7638391 0.94569
NM_001349338.3(FOXP1):c.-11-33T>A rs9855825 0.68941
NM_001349338.3(FOXP1):c.1722+137A>G rs9874207 0.63398
NM_001349338.3(FOXP1):c.181-213C>T rs3843363 0.58729
NM_001349338.3(FOXP1):c.1146+151T>C rs6802472 0.43060
NM_001349338.3(FOXP1):c.974+269A>T rs11128203 0.38769
NM_001349338.3(FOXP1):c.180+537A>T rs2293138 0.35336
NM_001349338.3(FOXP1):c.283-212A>G rs1288979 0.26965
NM_001349338.3(FOXP1):c.180+435G>A rs2293137 0.18945
NM_001349338.3(FOXP1):c.180+49T>C rs2037474 0.18939
NM_001349338.3(FOXP1):c.-91G>A rs17008544 0.15079
NM_001349338.3(FOXP1):c.420+243A>G rs1871148 0.12393
NM_001349338.3(FOXP1):c.180+96T>C rs939845 0.09446
NM_001349338.3(FOXP1):c.1652+806A>C rs3755733 0.07934
NM_001349338.3(FOXP1):c.-11-64C>T rs78495442 0.05088
NM_001349338.3(FOXP1):c.-11-52C>T rs78369780 0.04524
NM_001349338.3(FOXP1):c.1428+90G>C rs11924812 0.03826
NM_001349338.3(FOXP1):c.1889+149A>G rs17008086 0.03565
NM_001349338.3(FOXP1):c.1890-15G>T rs7639736 0.03466
NM_001349338.3(FOXP1):c.975-231G>A rs17008125 0.03253
NM_001349338.3(FOXP1):c.181-50C>T rs17008224 0.03159
NM_001349338.3(FOXP1):c.974+133G>A rs17008134 0.03063
NM_001349338.3(FOXP1):c.664+264C>T rs1288976 0.03005
NM_001349338.3(FOXP1):c.181-321C>G rs9985362 0.02935
NM_001349338.3(FOXP1):c.181-18054A>G rs58847217 0.02361
NM_001349338.3(FOXP1):c.1889+205A>G rs11928045 0.02166
NM_001349338.3(FOXP1):c.181-13T>G rs139264797 0.00220
NM_001349338.3(FOXP1):c.1702C>T (p.Pro568Ser) rs147674680 0.00185
NM_001349338.3(FOXP1):c.1709A>G (p.Asn570Ser) rs140161845 0.00140
NM_001349338.3(FOXP1):c.643C>G (p.Pro215Ala) rs146606219 0.00118
NM_001349338.3(FOXP1):c.1825G>A (p.Ala609Thr) rs147537388 0.00067
NM_001349338.3(FOXP1):c.1333G>A (p.Val445Met) rs147756430 0.00044
NM_001349338.3(FOXP1):c.1762G>A (p.Ala588Thr) rs202173892 0.00034
NM_001349338.3(FOXP1):c.44C>T (p.Ala15Val) rs532329866 0.00015
NM_001349338.3(FOXP1):c.1233C>T (p.Thr411=) rs147995584 0.00004
NM_001349338.3(FOXP1):c.*56dup rs112773801
NM_001349338.3(FOXP1):c.-11-29T>A rs56850311
NM_001349338.3(FOXP1):c.1062+128ATTTT[11] rs59993750
NM_001349338.3(FOXP1):c.1062+128ATTTT[12] rs59993750
NM_001349338.3(FOXP1):c.1062+128ATTTT[13] rs59993750
NM_001349338.3(FOXP1):c.870-74dup rs151011253

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