List of variants in gene combination FOXP1, LOC126806714 reported as likely benign

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 24

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HGVS	dbSNP	gnomAD frequency
NM_001349338.3(FOXP1):c.1429-70C>T	rs141214190	0.00445
NM_001349338.3(FOXP1):c.1530+13A>G	rs373765059	0.00009
NM_001349338.3(FOXP1):c.1515C>T (p.Asn505=)	rs201212255	0.00006
NM_001349338.3(FOXP1):c.1473C>T (p.Ile491=)	rs763824704	0.00002
NM_001349338.3(FOXP1):c.1518G>A (p.Ala506=)	rs776380840	0.00002
NM_001349338.3(FOXP1):c.1429-18T>C	rs183342745	0.00001
NM_001349338.3(FOXP1):c.1429-20T>C	rs780420927	0.00001
NM_001349338.3(FOXP1):c.1437C>T (p.Leu479=)	rs191080383	0.00001
NM_001349338.3(FOXP1):c.1456C>T (p.Leu486=)	rs1472132883	0.00001
NM_001349338.3(FOXP1):c.1489C>G (p.Arg497Gly)	rs775136381	0.00001
NM_001349338.3(FOXP1):c.1524G>A (p.Thr508=)	rs770674318	0.00001
NM_001349338.3(FOXP1):c.1530+14G>A	rs1305592943	0.00001
NM_001349338.3(FOXP1):c.1530+15G>A	rs1297616637	0.00001
NM_001349338.3(FOXP1):c.1429-11C>G	rs1026259010
NM_001349338.3(FOXP1):c.1429-14A>C
NM_001349338.3(FOXP1):c.1429-19G>C	rs2545111243
NM_001349338.3(FOXP1):c.1488A>T (p.Thr496=)	rs2545109950
NM_001349338.3(FOXP1):c.1503C>T (p.Tyr501=)
NM_001349338.3(FOXP1):c.1506C>T (p.Phe502=)
NM_001349338.3(FOXP1):c.1507C>A (p.Arg503=)
NM_001349338.3(FOXP1):c.1521C>T (p.Ala507=)	rs2545109462
NM_001349338.3(FOXP1):c.1530+12C>T	rs2545109138
NM_001349338.3(FOXP1):c.1530+16C>G	rs2545109019
NM_001349338.3(FOXP1):c.1530+17C>A

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