List of variants in gene KLF11 reported as benign for pancreas 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: 27

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HGVS	dbSNP	gnomAD frequency
NM_003597.5(KLF11):c.*1558T>C	rs4669522	0.82295
NM_003597.5(KLF11):c.*1853T>C	rs7632	0.55083
NM_003597.5(KLF11):c.*544C>A	rs4444493	0.08457
NM_003597.5(KLF11):c.*435A>T	rs72786612	0.07883
NM_003597.5(KLF11):c.*1781T>C	rs6722205	0.02856
NM_003597.5(KLF11):c.659C>T (p.Thr220Met)	rs34336420	0.01310
NM_003597.5(KLF11):c.*194G>A	rs76220150	0.00789
NM_003597.5(KLF11):c.*235T>C	rs150051327	0.00733
NM_003597.5(KLF11):c.429C>T (p.Ala143=)	rs113903638	0.00679
NM_003597.5(KLF11):c.*107G>A	rs140559044	0.00616
NM_003597.5(KLF11):c.*981G>A	rs148235172	0.00584
NM_003597.5(KLF11):c.*882G>A	rs183240123	0.00564
NM_003597.5(KLF11):c.*262C>T	rs147746428	0.00373
NM_003597.5(KLF11):c.410A>G (p.Asp137Gly)	rs145933214	0.00328
NM_003597.5(KLF11):c.*241A>G	rs191010106	0.00309
NM_003597.5(KLF11):c.*980T>C	rs113527829	0.00303
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.*2144C>T	rs139703378	0.00157
NM_003597.5(KLF11):c.*2026G>C	rs146068438	0.00152
NM_003597.5(KLF11):c.1205G>A (p.Arg402Gln)	rs34762805	0.00088
NM_003597.5(KLF11):c.*612C>T	rs187519040	0.00045
NM_003597.5(KLF11):c.1448C>T (p.Pro483Leu)	rs201735305	0.00023
NM_003597.5(KLF11):c.1450G>A (p.Gly484Ser)	rs750063435	0.00006
NM_003597.5(KLF11):c.*192T>C	rs552960564	0.00001
NM_003597.5(KLF11):c.*1423T>C	rs571234569
NM_003597.5(KLF11):c.226_227dup	rs34206941

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