ClinVar Miner

Variants in gene KCNJ2 with conflicting interpretations

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
112 117 0 9 4 0 7 19

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 0 2 5 0 0
likely pathogenic 2 0 3 0 0
uncertain significance 5 3 0 4 0
likely benign 0 0 4 0 7
benign 0 0 0 7 0

All variants with conflicting interpretations #

Total variants: 19
Download table as spreadsheet
HGVS dbSNP
NM_000891.2(KCNJ2):c.-228C>T rs765064661
NM_000891.2(KCNJ2):c.-2C>T rs144760658
NM_000891.2(KCNJ2):c.1044C>T (p.Tyr348=) rs146330042
NM_000891.2(KCNJ2):c.1065T>G (p.Leu355=) rs139564374
NM_000891.2(KCNJ2):c.1229A>G (p.Asn410Ser) rs141069645
NM_000891.2(KCNJ2):c.168T>C (p.Val56=) rs370111593
NM_000891.2(KCNJ2):c.174C>T (p.Phe58=) rs587781006
NM_000891.2(KCNJ2):c.213C>T (p.Asp71=) rs150671256
NM_000891.2(KCNJ2):c.226T>G (p.Cys76Gly) rs786205812
NM_000891.2(KCNJ2):c.245G>A (p.Arg82Gln) rs199473653
NM_000891.2(KCNJ2):c.261C>T (p.Ile87=) rs1166497262
NM_000891.2(KCNJ2):c.277G>A (p.Val93Ile) rs147750704
NM_000891.2(KCNJ2):c.531C>T (p.Gly177=) rs544384907
NM_000891.2(KCNJ2):c.867C>T (p.Asn289=) rs201909993
NM_000891.2(KCNJ2):c.901A>C (p.Met301Leu) rs786205818
NM_000891.2(KCNJ2):c.901A>G (p.Met301Val) rs786205818
NM_000891.2(KCNJ2):c.919A>G (p.Met307Val) rs1555603994
NM_000891.2(KCNJ2):c.935G>A (p.Arg312His) rs786205820
NM_000891.2(KCNJ2):c.953A>G (p.Asn318Ser) rs367560052

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