ClinVar Miner

List of variants in gene ABCC2 reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 16
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HGVS dbSNP
NM_000392.5(ABCC2):c.-24C>T rs717620
NM_000392.5(ABCC2):c.1058G>A (p.Arg353His) rs7080681
NM_000392.5(ABCC2):c.1219C>T (p.Leu407=) rs17216198
NM_000392.5(ABCC2):c.1446C>G (p.Thr482=) rs113646094
NM_000392.5(ABCC2):c.2546T>G (p.Leu849Arg) rs17222617
NM_000392.5(ABCC2):c.2883+11C>T rs41318031
NM_000392.5(ABCC2):c.3542G>T (p.Arg1181Leu) rs8187692
NM_000392.5(ABCC2):c.3563T>A (p.Val1188Glu) rs17222723
NM_000392.5(ABCC2):c.4062C>T (p.Ala1354=) rs17216275
NM_000392.5(ABCC2):c.4110C>T (p.Leu1370=) rs7899457
NM_000392.5(ABCC2):c.4146+11G>C rs17216282
NM_000392.5(ABCC2):c.4290G>T (p.Val1430=) rs1137968
NM_000392.5(ABCC2):c.4410G>A (p.Glu1470=) rs8187706
NM_000392.5(ABCC2):c.4488C>T (p.His1496=) rs8187707
NM_000392.5(ABCC2):c.4508+12G>A rs17216212
NM_000392.5(ABCC2):c.4544G>A (p.Cys1515Tyr) rs8187710

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