ClinVar Miner

List of variants in gene WDR35 reported as benign for Cranioectodermal dysplasia 2; Short rib polydactyly syndrome 5

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Total variants: 16
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HGVS dbSNP
NM_020779.4(WDR35):c.1058G>C (p.Arg353Pro) rs76623454
NM_020779.4(WDR35):c.1089G>A (p.Thr363=) rs79829477
NM_020779.4(WDR35):c.1195-1693A>G rs144673252
NM_020779.4(WDR35):c.1471-7A>G rs376388391
NM_020779.4(WDR35):c.1591C>G (p.Leu531Val) rs148242353
NM_020779.4(WDR35):c.1601G>A (p.Arg534Gln) rs113345685
NM_020779.4(WDR35):c.1755C>T (p.Val585=) rs146130105
NM_020779.4(WDR35):c.2149A>G (p.Ile717Val) rs144493712
NM_020779.4(WDR35):c.2262C>T (p.Asp754=) rs147206032
NM_020779.4(WDR35):c.2566G>T (p.Val856Phe) rs149667250
NM_020779.4(WDR35):c.2835A>G (p.Glu945=) rs182928585
NM_020779.4(WDR35):c.3019C>T (p.Arg1007Cys) rs56395266
NM_020779.4(WDR35):c.318T>C (p.Ile106=) rs115963122
NM_020779.4(WDR35):c.3279G>C (p.Gln1093His) rs148436608
NM_020779.4(WDR35):c.549C>T (p.Tyr183=) rs34169020
NM_020779.4(WDR35):c.765C>T (p.Tyr255=) rs117255034

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