ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
Download table as spreadsheet
NM_020779.4(WDR35):c.1183A>T (p.Asn395Tyr) rs143343508
NM_020779.4(WDR35):c.1195-1705C>T rs142103808
NM_020779.4(WDR35):c.1248T>G (p.Ile416Met) rs144701688
NM_020779.4(WDR35):c.1860C>T (p.Thr620=) rs1572333836
NM_020779.4(WDR35):c.2066G>A (p.Arg689His) rs74470618
NM_020779.4(WDR35):c.2326C>T (p.Leu776=) rs772138388
NM_020779.4(WDR35):c.2777A>G (p.Tyr926Cys) rs75602337
NM_020779.4(WDR35):c.2964+10C>A rs201207790
NM_020779.4(WDR35):c.3121+3G>A rs200042577
NM_020779.4(WDR35):c.3252G>A (p.Glu1084=) rs182360785
NM_020779.4(WDR35):c.3335A>G (p.Lys1112Arg) rs138007924
NM_020779.4(WDR35):c.3467T>G (p.Ile1156Arg) rs147325795
NM_020779.4(WDR35):c.355C>T (p.Arg119Cys) rs140308808
NM_020779.4(WDR35):c.681T>C (p.Leu227=) rs143901897
NM_020779.4(WDR35):c.725A>G (p.Glu242Gly) rs139543775
NM_020779.4(WDR35):c.761T>C (p.Met254Thr) rs547986777
NM_020779.4(WDR35):c.770T>C (p.Val257Ala) rs142955097

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.