List of variants in gene KLF11 reported as likely benign for digestive system disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 22

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HGVS	dbSNP	gnomAD frequency
NM_003597.5(KLF11):c.185A>G (p.Gln62Arg)	rs35927125	0.08880
NM_003597.5(KLF11):c.659C>T (p.Thr220Met)	rs34336420	0.01310
NM_003597.5(KLF11):c.86G>A (p.Arg29Gln)	rs150096859	0.00188
NM_003597.5(KLF11):c.782C>T (p.Pro261Leu)	rs148123124	0.00170
NM_003597.5(KLF11):c.541G>A (p.Glu181Lys)	rs146238335	0.00163
NM_003597.5(KLF11):c.225C>T (p.Val75=)	rs144083374	0.00158
NM_003597.5(KLF11):c.486A>G (p.Pro162=)	rs146462049	0.00093
NM_003597.5(KLF11):c.1205G>A (p.Arg402Gln)	rs34762805	0.00088
NM_003597.5(KLF11):c.953T>G (p.Leu318Arg)	rs144431930	0.00048
NM_003597.5(KLF11):c.1503G>A (p.Pro501=)	rs36091043	0.00040
NM_003597.5(KLF11):c.546C>A (p.Ser182Arg)	rs142266428	0.00019
NM_003597.5(KLF11):c.*982G>A	rs550807244	0.00017
NM_003597.5(KLF11):c.*2274G>A	rs149368043	0.00012
NM_003597.5(KLF11):c.1039G>T (p.Ala347Ser)	rs121912645	0.00009
NM_003597.5(KLF11):c.1161C>T (p.Asp387=)	rs117449189	0.00008
NM_003597.5(KLF11):c.1130C>T (p.Thr377Ile)	rs370236540	0.00006
NM_003597.5(KLF11):c.679A>G (p.Asn227Asp)	rs200561467	0.00006
NM_003597.5(KLF11):c.*122C>T	rs576978858
NM_003597.5(KLF11):c.*227dup	rs34206941
NM_003597.5(KLF11):c.1050G>A (p.Pro350=)	rs145193520
NM_003597.5(KLF11):c.42+18C>G	rs1476684022
NM_003597.5(KLF11):c.870C>T (p.Ile290=)	rs149235463

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