ClinVar Miner

List of variants in gene WDR35 reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 24
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HGVS dbSNP
NM_001006657.2(WDR35):c.*1050T>C rs10197890
NM_001006657.2(WDR35):c.*1127A>G rs75503594
NM_001006657.2(WDR35):c.*1129C>T rs76845713
NM_001006657.2(WDR35):c.*1479C>T rs77400381
NM_001006657.2(WDR35):c.*1489G>A rs10182866
NM_001006657.2(WDR35):c.*1575_*1576dup rs202074829
NM_001006657.2(WDR35):c.*2408G>C rs112569580
NM_001006657.2(WDR35):c.*2463C>T rs3731661
NM_001006657.2(WDR35):c.*2836C>T rs74469198
NM_001006657.2(WDR35):c.*2957G>A rs76072774
NM_001006657.2(WDR35):c.*3268C>T rs113280329
NM_001006657.2(WDR35):c.*553G>T rs79153401
NM_001006657.2(WDR35):c.*98T>C rs6748924
NM_001006657.2(WDR35):c.1281T>G (p.Ile427Met) rs144701688
NM_001006657.2(WDR35):c.1634G>A (p.Arg545Gln) rs113345685
NM_001006657.2(WDR35):c.2099G>A (p.Arg700His) rs74470618
NM_001006657.2(WDR35):c.2182A>G (p.Ile728Val) rs144493712
NM_001006657.2(WDR35):c.2599G>T (p.Val867Phe) rs149667250
NM_001006657.2(WDR35):c.2632G>A (p.Ala878Thr) rs2293669
NM_001006657.2(WDR35):c.3154+12A>C rs28502265
NM_001006657.2(WDR35):c.549C>T (p.Tyr183=) rs34169020
NM_001006657.2(WDR35):c.666T>A (p.Pro222=) rs987346249
NM_001006657.2(WDR35):c.725A>G (p.Glu242Gly) rs139543775
NM_001006657.2(WDR35):c.770T>C (p.Val257Ala) rs142955097

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