ClinVar Miner

List of variants in gene KCNJ11 reported as uncertain significance for carbohydrate metabolism disease

Included ClinVar conditions (161):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 80
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HGVS dbSNP
NM_000525.3(KCNJ11):c.*1055T>A rs886048032
NM_000525.3(KCNJ11):c.*1168G>A rs182349583
NM_000525.3(KCNJ11):c.*1197G>A rs191682072
NM_000525.3(KCNJ11):c.*1562A>G rs886048031
NM_000525.3(KCNJ11):c.*218G>T rs886048039
NM_000525.3(KCNJ11):c.*288G>A rs5209
NM_000525.3(KCNJ11):c.*311C>T rs886048038
NM_000525.3(KCNJ11):c.*376C>T rs5208
NM_000525.3(KCNJ11):c.*40C>T rs746850899
NM_000525.3(KCNJ11):c.*487A>G rs79457490
NM_000525.3(KCNJ11):c.*50G>A rs886048041
NM_000525.3(KCNJ11):c.*529G>A rs115826080
NM_000525.3(KCNJ11):c.*546G>A rs886048037
NM_000525.3(KCNJ11):c.*678C>T rs886048036
NM_000525.3(KCNJ11):c.*686A>G rs147282653
NM_000525.3(KCNJ11):c.*697G>A rs117976105
NM_000525.3(KCNJ11):c.*701A>T rs5207
NM_000525.3(KCNJ11):c.*732C>T rs886048035
NM_000525.3(KCNJ11):c.*76G>A rs193076739
NM_000525.3(KCNJ11):c.*862G>T rs547635594
NM_000525.3(KCNJ11):c.*92C>T rs5212
NM_000525.3(KCNJ11):c.*937C>T rs886048033
NM_000525.3(KCNJ11):c.*99C>G rs886048040
NM_000525.3(KCNJ11):c.-135_-134insCT rs1554901983
NM_000525.3(KCNJ11):c.-150G>A rs886048043
NM_000525.3(KCNJ11):c.-179C>T rs776949660
NM_000525.3(KCNJ11):c.-515G>A rs886048044
NM_000525.3(KCNJ11):c.-546G>T rs886048045
NM_000525.3(KCNJ11):c.-54C>T rs1016780684
NM_000525.3(KCNJ11):c.1016T>G (p.Val339Gly) rs138125678
NM_000525.3(KCNJ11):c.1034C>T (p.Thr345Met) rs114215135
NM_000525.3(KCNJ11):c.1040G>A (p.Arg347His) rs771797701
NM_000525.3(KCNJ11):c.1064T>C (p.Leu355Pro) rs797045635
NM_000525.3(KCNJ11):c.1093C>T (p.Arg365Cys) rs758749160
NM_000525.3(KCNJ11):c.1094G>A (p.Arg365His) rs750689750
NM_000525.3(KCNJ11):c.1095C>T (p.Arg365=) rs143276279
NM_000525.3(KCNJ11):c.1112G>A (p.Arg371His) rs1233061680
NM_000525.3(KCNJ11):c.1138_1143dup (p.Lys381_Phe382insProLys) rs1440128889
NM_000525.3(KCNJ11):c.1143G>A (p.Lys381=) rs8175351
NM_000525.3(KCNJ11):c.1154C>G (p.Ser385Cys) rs41282930
NM_000525.3(KCNJ11):c.119G>A (p.Gly40Asp) rs1001873841
NM_000525.3(KCNJ11):c.161G>A (p.Arg54His) rs587783666
NM_000525.3(KCNJ11):c.264G>T (p.Met88Ile) rs1554901866
NM_000525.3(KCNJ11):c.292G>A (p.Gly98Ser) rs1554901851
NM_000525.3(KCNJ11):c.302C>A (p.Ala101Asp) rs1014454531
NM_000525.3(KCNJ11):c.407G>A (p.Arg136His) rs1479483693
NM_000525.3(KCNJ11):c.525C>A (p.His175Gln) rs865963367
NM_000525.3(KCNJ11):c.527G>A (p.Arg176His) rs1266231295
NM_000525.3(KCNJ11):c.575G>A (p.Arg192His) rs750778014
NM_000525.3(KCNJ11):c.584G>A (p.Arg195His) rs5217
NM_000525.3(KCNJ11):c.617G>T (p.Arg206Leu) rs1554901747
NM_000525.3(KCNJ11):c.662G>A (p.Arg221His) rs768909861
NM_000525.3(KCNJ11):c.741C>T (p.Asn247=) rs886048042
NM_000525.3(KCNJ11):c.797C>T (p.Pro266Leu) rs1554901679
NM_000525.3(KCNJ11):c.801C>G (p.Leu267=) rs5216
NM_000525.3(KCNJ11):c.80G>A (p.Arg27His) rs774714794
NM_000525.3(KCNJ11):c.819C>T (p.Ser273=) rs202238153
NM_000525.3(KCNJ11):c.841_843del (p.Leu281del) rs1554901658
NM_000525.3(KCNJ11):c.843C>T (p.Leu281=) rs116392938
NM_000525.3(KCNJ11):c.853G>A (p.Val285Ile) rs149667199
NM_000525.3(KCNJ11):c.902G>A (p.Arg301His) rs74339576
NM_000525.3(KCNJ11):c.970G>A (p.Gly324Arg) rs1193170151
NM_000525.3(KCNJ11):c.973C>A (p.Arg325Ser) rs550315112
NM_000525.4(KCNJ11):c.*1037G>T
NM_000525.4(KCNJ11):c.*1220G>A
NM_000525.4(KCNJ11):c.*1415G>A
NM_000525.4(KCNJ11):c.*766G>A
NM_000525.4(KCNJ11):c.*842C>G
NM_000525.4(KCNJ11):c.*848A>G
NM_000525.4(KCNJ11):c.*849C>G
NM_000525.4(KCNJ11):c.-37C>T
NM_000525.4(KCNJ11):c.-424C>T
NM_000525.4(KCNJ11):c.1172G>A (p.Ter391=)
NM_000525.4(KCNJ11):c.156G>A (p.Gln52=)
NM_000525.4(KCNJ11):c.451G>A (p.Val151Met)
NM_000525.4(KCNJ11):c.463G>A rs587783668
NM_000525.4(KCNJ11):c.79C>T rs752507753
NM_000525.4(KCNJ11):c.804C>T rs778225010
NM_000525.4(KCNJ11):c.83C>T (p.Ala28Val)
NM_000525.4(KCNJ11):c.91C>T (p.Arg31Trp)

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