ClinVar Miner

List of variants in gene WDR35 reported as benign for syndromic craniosynostosis

Included ClinVar conditions (70):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_020779.4(WDR35):c.2824-14G>T rs1191779 0.96807
NM_020779.4(WDR35):c.25-46G>A rs3731663 0.57247
NM_020779.4(WDR35):c.2496A>G (p.Glu832=) rs6741091 0.45165
NM_020779.4(WDR35):c.2915A>G (p.Glu972Gly) rs1191778 0.31383
NM_020779.4(WDR35):c.*523G>A rs957614 0.25621
NM_020779.4(WDR35):c.*231C>A rs1056233 0.25618
NM_020779.4(WDR35):c.3121+12A>C rs28502265 0.10214
NM_020779.4(WDR35):c.*1050T>C rs10197890 0.10201
NM_020779.4(WDR35):c.*98T>C rs6748924 0.10155
NM_020779.4(WDR35):c.*2463C>T rs3731661 0.07941
NM_020779.4(WDR35):c.2599G>A (p.Ala867Thr) rs2293669 0.05563
NM_020779.4(WDR35):c.*1489G>A rs10182866 0.05128
NM_020779.4(WDR35):c.*1127A>G rs75503594 0.04161
NM_020779.4(WDR35):c.*2957G>A rs76072774 0.03646
NM_020779.4(WDR35):c.549C>T (p.Tyr183=) rs34169020 0.03645
NM_020779.4(WDR35):c.*2836C>T rs74469198 0.02096
NM_020779.4(WDR35):c.*2408G>C rs112569580 0.01898
NM_020779.4(WDR35):c.*3268C>T rs113280329 0.01807
NM_020779.4(WDR35):c.*1479C>T rs77400381 0.01800
NM_020779.4(WDR35):c.*1129C>T rs76845713 0.01385
NM_020779.4(WDR35):c.*553G>T rs79153401 0.01323
NM_020779.4(WDR35):c.1601G>A (p.Arg534Gln) rs113345685 0.01206
NM_020779.4(WDR35):c.3019C>T (p.Arg1007Cys) rs56395266 0.01130
NM_020779.4(WDR35):c.1089G>A (p.Thr363=) rs79829477 0.00817
NM_020779.4(WDR35):c.*1406A>G rs10197681 0.00613
NM_020779.4(WDR35):c.2414+20C>T rs116756504 0.00361
NM_020779.4(WDR35):c.2262C>T (p.Asp754=) rs147206032 0.00285
NM_020779.4(WDR35):c.318T>C (p.Ile106=) rs115963122 0.00263
NM_020779.4(WDR35):c.2964+12C>T rs113663112 0.00252
NM_020779.4(WDR35):c.1591C>G (p.Leu531Val) rs148242353 0.00233
NM_020779.4(WDR35):c.1524+11C>A rs200213874 0.00201
NM_020779.4(WDR35):c.3279G>C (p.Gln1093His) rs148436608 0.00161
NM_020779.4(WDR35):c.1755C>T (p.Val585=) rs146130105 0.00124
NM_020779.4(WDR35):c.*2623T>C rs538967974 0.00121
NM_020779.4(WDR35):c.*2622A>G rs558837510 0.00116
NM_020779.4(WDR35):c.1471-7A>G rs376388391 0.00098
NM_020779.4(WDR35):c.437-13T>C rs367802842 0.00098
NM_020779.4(WDR35):c.142+10T>C rs186647997 0.00096
NM_020779.4(WDR35):c.507A>G (p.Lys169=) rs200495720 0.00094
NM_020779.4(WDR35):c.2149A>G (p.Ile717Val) rs144493712 0.00089
NM_020779.4(WDR35):c.853A>T (p.Ile285Phe) rs200059077 0.00073
NM_020779.4(WDR35):c.1401-15T>G rs201903683 0.00068
NM_020779.4(WDR35):c.*487C>T rs116951767 0.00056
NM_020779.4(WDR35):c.765C>T (p.Tyr255=) rs117255034 0.00013
NM_001006657.2(WDR35):c.1215A>G (p.Thr405=) rs144673252 0.00011
NM_020779.4(WDR35):c.2835A>G (p.Glu945=) rs182928585 0.00010
NM_020779.4(WDR35):c.867C>T (p.Tyr289=) rs185888517 0.00008
NM_020779.4(WDR35):c.1053T>C (p.Pro351=) rs74385826 0.00004
NM_020779.4(WDR35):c.1845+16G>A rs376710057 0.00001
NM_020779.4(WDR35):c.*978A>G rs149444449
NM_020779.4(WDR35):c.1058G>C (p.Arg353Pro) rs76623454
NM_020779.4(WDR35):c.1846-11dup rs754138477
NM_020779.4(WDR35):c.24+17dup
NM_020779.4(WDR35):c.2622A>T (p.Pro874=)

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