ClinVar Miner

List of variants in gene WDR4 reported as benign for autosomal recessive disease

Included ClinVar conditions (1198):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_018669.6(WDR4):c.213G>C (p.Lys71Asn) rs2248490 0.55249
NM_018669.6(WDR4):c.796C>T (p.Pro266Ser) rs15736 0.44094
NM_018669.6(WDR4):c.1169G>A (p.Arg390Gln) rs6586250 0.24647
NM_018669.6(WDR4):c.1045+38C>T rs8133179 0.19799
NM_018669.6(WDR4):c.567-16T>C rs7278765 0.17080

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