ClinVar Miner

Variants in gene WDR19 with conflicting interpretations

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Y axis minimum submission review status: Y axis collection method:
X axis minimum submission review status: X axis collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than two submissions, it may have multiple conflicts and therefore be counted in more than one conflict column. If this is the case, the "Variants with any kind of conflict" cell will be less than the sum of the conflicted variants cells to its left.

Variants with only 1 submission Variants with at least 2 submissions and no conflicts Variants with a synonymous conflict
(e.g. benign vs non-pathogenic)
Variants with a confidence conflict
(e.g. benign vs likely benign)
Variants with a benign or likely benign vs uncertain conflict Variants with a category conflict
(e.g. benign vs affects)
Variants with a clinically significant conflict
(e.g. benign vs pathogenic)
Variants with any kind of conflict
76 49 2 8 6 0 2 16

Significance breakdown #

In the table below, cells that correspond to a term paired with itself represent synonymous conflicts, i.e. variants that have been annotated with different terms that map to the same standard term. To compare the terms that were actually submitted, check the box in the filters section at the top of this page.

pathogenic likely pathogenic uncertain significance likely benign benign
pathogenic 2 1 2 0 0
likely pathogenic 1 0 1 0 0
uncertain significance 2 1 0 5 2
likely benign 0 0 5 0 7
benign 0 0 2 7 0

All variants with conflicting interpretations #

Total variants: 16
Download table as spreadsheet
HGVS dbSNP
NM_025132.4(WDR19):c.-9A>G rs60800612
NM_025132.4(WDR19):c.1198C>T (p.Leu400=) rs199765304
NM_025132.4(WDR19):c.1357-10T>C rs16995189
NM_025132.4(WDR19):c.1595T>C (p.Ile532Thr) rs749672769
NM_025132.4(WDR19):c.1915A>G (p.Ser639Gly) rs150649460
NM_025132.4(WDR19):c.2129T>C (p.Leu710Ser) rs387906980
NM_025132.4(WDR19):c.2361C>T (p.Phe787=) rs200133722
NM_025132.4(WDR19):c.2671C>T (p.His891Tyr) rs200266424
NM_025132.4(WDR19):c.2715G>A (p.Lys905=) rs200339331
NM_025132.4(WDR19):c.2792A>C (p.Tyr931Ser) rs187546086
NM_025132.4(WDR19):c.3250G>A (p.Gly1084Ser) rs16995209
NM_025132.4(WDR19):c.3307C>T (p.Arg1103Ter) rs387906981
NM_025132.4(WDR19):c.3533G>A (p.Arg1178Gln) rs79436363
NM_025132.4(WDR19):c.781dup (p.Thr261fs) rs748656635
NM_025132.4(WDR19):c.852A>G (p.Ser284=) rs17584431
NM_025132.4(WDR19):c.910G>A (p.Val304Ile) rs75964850

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