ClinVar Miner

List of variants in gene WDR19 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (916):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 56
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HGVS dbSNP
NM_025132.4(WDR19):c.*131C>T rs886059404
NM_025132.4(WDR19):c.*152G>A rs533059483
NM_025132.4(WDR19):c.*184T>G rs886059405
NM_025132.4(WDR19):c.*293_*296dup rs374474677
NM_025132.4(WDR19):c.-15G>T rs150860929
NM_025132.4(WDR19):c.1064A>T (p.Asp355Val) rs192495145
NM_025132.4(WDR19):c.1134+13T>G rs374615138
NM_025132.4(WDR19):c.1173C>T (p.Asn391=) rs777985189
NM_025132.4(WDR19):c.1198C>T (p.Leu400=) rs199765304
NM_025132.4(WDR19):c.1248T>C (p.Asn416=) rs772867899
NM_025132.4(WDR19):c.1249+9A>G rs201377206
NM_025132.4(WDR19):c.1293C>T (p.Ala431=) rs886059397
NM_025132.4(WDR19):c.13+14C>T rs758352852
NM_025132.4(WDR19):c.13+15G>A rs150633358
NM_025132.4(WDR19):c.1357-7G>A rs377101599
NM_025132.4(WDR19):c.1390C>T (p.Arg464Cys) rs201148758
NM_025132.4(WDR19):c.1595T>C (p.Ile532Thr) rs749672769
NM_025132.4(WDR19):c.1839A>G (p.Leu613=) rs201320006
NM_025132.4(WDR19):c.1932G>A (p.Thr644=) rs886059398
NM_025132.4(WDR19):c.198A>T (p.Gly66=) rs749815295
NM_025132.4(WDR19):c.2003T>C (p.Met668Thr)
NM_025132.4(WDR19):c.2142+12G>A rs149621476
NM_025132.4(WDR19):c.2218T>C (p.Tyr740His) rs886059399
NM_025132.4(WDR19):c.2361C>T (p.Phe787=) rs200133722
NM_025132.4(WDR19):c.2364-15T>C rs771036360
NM_025132.4(WDR19):c.2364-15_2364-14del rs555557314
NM_025132.4(WDR19):c.2429A>G (p.Asp810Gly) rs886059400
NM_025132.4(WDR19):c.2782A>T (p.Ile928Phe) rs780963454
NM_025132.4(WDR19):c.2792A>C (p.Tyr931Ser) rs187546086
NM_025132.4(WDR19):c.3016A>G (p.Thr1006Ala) rs199678654
NM_025132.4(WDR19):c.3160G>T (p.Ala1054Ser)
NM_025132.4(WDR19):c.3183+9G>A rs138318063
NM_025132.4(WDR19):c.3249T>C (p.Asp1083=) rs371128500
NM_025132.4(WDR19):c.3283T>C (p.Leu1095=) rs769329045
NM_025132.4(WDR19):c.3358+15C>T rs750722358
NM_025132.4(WDR19):c.3362A>G (p.Asn1121Ser) rs545916111
NM_025132.4(WDR19):c.3383T>C (p.Val1128Ala) rs372799054
NM_025132.4(WDR19):c.3416A>G (p.Gln1139Arg) rs75621037
NM_025132.4(WDR19):c.3439A>G (p.Met1147Val) rs886059401
NM_025132.4(WDR19):c.3533G>A (p.Arg1178Gln) rs79436363
NM_025132.4(WDR19):c.3602G>A (p.Cys1201Tyr) rs886059402
NM_025132.4(WDR19):c.3667C>T (p.Arg1223Cys) rs201597047
NM_025132.4(WDR19):c.3722C>T (p.Pro1241Leu) rs576113399
NM_025132.4(WDR19):c.3758G>A (p.Cys1253Tyr) rs750716949
NM_025132.4(WDR19):c.3775C>A (p.Leu1259Ile) rs886059403
NM_025132.4(WDR19):c.3784G>A (p.Glu1262Lys) rs1553919125
NM_025132.4(WDR19):c.3808T>A (p.Cys1270Ser) rs1035768119
NM_025132.4(WDR19):c.3936C>T (p.Ser1312=)
NM_025132.4(WDR19):c.523-3T>C rs747603843
NM_025132.4(WDR19):c.56T>G (p.Phe19Cys) rs1247231925
NM_025132.4(WDR19):c.6+5A>G rs201198839
NM_025132.4(WDR19):c.750A>T (p.Ser250=) rs886059395
NM_025132.4(WDR19):c.929A>G (p.Tyr310Cys) rs199783864
NM_025132.4(WDR19):c.935T>C (p.Ile312Thr) rs886059396
NM_025132.4(WDR19):c.959A>T (p.Lys320Ile)
NM_025132.4(WDR19):c.974T>C (p.Leu325Ser) rs1193255568

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