ClinVar Miner

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

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
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HGVS dbSNP
NM_020779.4(WDR35):c.*1050T>C rs10197890
NM_020779.4(WDR35):c.*1127A>G rs75503594
NM_020779.4(WDR35):c.*1129C>T rs76845713
NM_020779.4(WDR35):c.*1479C>T rs77400381
NM_020779.4(WDR35):c.*1489G>A rs10182866
NM_020779.4(WDR35):c.*1575_*1576dup rs202074829
NM_020779.4(WDR35):c.*2408G>C rs112569580
NM_020779.4(WDR35):c.*2463C>T rs3731661
NM_020779.4(WDR35):c.*2836C>T rs74469198
NM_020779.4(WDR35):c.*2957G>A rs76072774
NM_020779.4(WDR35):c.*3268C>T rs113280329
NM_020779.4(WDR35):c.*553G>T rs79153401
NM_020779.4(WDR35):c.*98T>C rs6748924
NM_020779.4(WDR35):c.1601G>A (p.Arg534Gln) rs113345685
NM_020779.4(WDR35):c.2149A>G (p.Ile717Val) rs144493712
NM_020779.4(WDR35):c.2566G>T (p.Val856Phe) rs149667250
NM_020779.4(WDR35):c.2599G>A (p.Ala867Thr) rs2293669
NM_020779.4(WDR35):c.3121+12A>C rs28502265
NM_020779.4(WDR35):c.549C>T (p.Tyr183=) rs34169020

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