ClinVar Miner

List of variants in gene WDR4 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_018669.6(WDR4):c.453+216A>G rs1888521 0.64408
NM_018669.6(WDR4):c.90-164C>T rs12626259 0.60209
NM_018669.6(WDR4):c.89+193C>G rs8127072 0.60176
NM_018669.6(WDR4):c.213G>C (p.Lys71Asn) rs2248490 0.54570
NM_018669.6(WDR4):c.90-57A>T rs7279447 0.51880
NM_018669.6(WDR4):c.796C>T (p.Pro266Ser) rs15736 0.44094
NM_018669.6(WDR4):c.727-109T>C rs1107831 0.43849
NM_018669.6(WDR4):c.1046-50G>C rs6586251 0.43741
NM_018669.6(WDR4):c.628-89A>G rs465663 0.43410
NM_018669.6(WDR4):c.1169G>A (p.Arg390Gln) rs6586250 0.24063
NM_018669.6(WDR4):c.1045+38C>T rs8133179 0.18964
NM_018669.6(WDR4):c.567-16T>C rs7278765 0.17080
NM_018669.6(WDR4):c.1046-149C>T rs883269 0.16914
NM_018669.6(WDR4):c.567-56C>T rs11909507 0.14249
NM_018669.6(WDR4):c.297-12C>T rs7279435 0.12565
NM_018669.6(WDR4):c.628-55C>T rs62215012 0.10775
NM_018669.6(WDR4):c.429G>A (p.Gly143=) rs11911090 0.10418
NM_018669.6(WDR4):c.90-83G>A rs11700660 0.09631
NM_018669.6(WDR4):c.791+30C>T rs2298666 0.05909
NM_018669.6(WDR4):c.297-79C>T rs112237505 0.05900
NM_018669.6(WDR4):c.792-145A>T rs460128 0.05621
NM_018669.6(WDR4):c.628-193C>T rs463183 0.05004
NM_018669.6(WDR4):c.566+54del rs144064922 0.04644
NM_018669.6(WDR4):c.1089C>T (p.Ala363=) rs17115515 0.04072
NM_018669.6(WDR4):c.296+112G>A rs112145119 0.01927
NM_018669.6(WDR4):c.296+152_296+153del rs139267801 0.01673
NM_018669.6(WDR4):c.976-174T>C rs113437360 0.01611
NM_018669.6(WDR4):c.300C>T (p.Thr100=) rs61729418 0.01606
NM_018669.6(WDR4):c.891C>T (p.Phe297=) rs61729406 0.00982
NM_018669.6(WDR4):c.976-9C>T rs112937323 0.00445
NM_018669.6(WDR4):c.792-9C>T rs199715637 0.00279
NM_018669.6(WDR4):c.633C>T (p.Gly211=) rs112027714 0.00269
NM_018669.6(WDR4):c.156-5C>T rs146400491 0.00082
NM_018669.6(WDR4):c.798T>C (p.Pro266=) rs200229841 0.00081
NM_018669.6(WDR4):c.861G>A (p.Ala287=) rs146066316 0.00054
NM_018669.6(WDR4):c.70G>T (p.Ala24Ser) rs150449975 0.00053
NM_018669.6(WDR4):c.138G>A (p.Lys46=) rs200785846 0.00011
NM_018669.6(WDR4):c.1122G>A (p.Lys374=) rs368777100
NM_018669.6(WDR4):c.33G>A (p.Gly11=) rs138295040
NM_018669.6(WDR4):c.627+84_627+85insCTGGCCCCGGTGGATCG rs796985028
NM_018669.6(WDR4):c.627+87_627+103dup rs149300976
NM_018669.6(WDR4):c.90-115C>T rs7283064
NM_018669.6(WDR4):c.90-57del rs71332377
NM_018669.6(WDR4):c.963C>T (p.Gly321=) rs146863277

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