ClinVar Miner

List of variants in gene ABCC2 studied for not specified

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Total variants: 19
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HGVS dbSNP
NM_000392.5(ABCC2):c.-24C>T rs717620
NM_000392.5(ABCC2):c.1249G>A (p.Val417Ile) rs2273697
NM_000392.5(ABCC2):c.1446C>G (p.Thr482=) rs113646094
NM_000392.5(ABCC2):c.1483A>G (p.Lys495Glu) rs17222561
NM_000392.5(ABCC2):c.159A>G (p.Lys53=) rs17222596
NM_000392.5(ABCC2):c.2073C>A (p.Val691=) rs17222624
NM_000392.5(ABCC2):c.2743C>T (p.Arg915Cys) rs112758556
NM_000392.5(ABCC2):c.2813G>A (p.Ser938Asn) rs112339372
NM_000392.5(ABCC2):c.2944A>G (p.Ile982Val) rs17222554
NM_000392.5(ABCC2):c.3026T>C (p.Ile1009Thr) rs57351269
NM_000392.5(ABCC2):c.3107T>C (p.Ile1036Thr) rs45441199
NM_000392.5(ABCC2):c.3188A>G (p.Asn1063Ser) rs17222540
NM_000392.5(ABCC2):c.3542G>T (p.Arg1181Leu) rs8187692
NM_000392.5(ABCC2):c.3872C>T (p.Pro1291Leu) rs17216317
NM_000392.5(ABCC2):c.3972C>T (p.Ile1324=) rs3740066
NM_000392.5(ABCC2):c.4509-9T>C rs180717330
NM_000392.5(ABCC2):c.4527C>T (p.Asn1509=) rs8187709
NM_000392.5(ABCC2):c.842G>A (p.Ser281Asn) rs56131651
NM_000392.5(ABCC2):c.867+8T>C rs74152764

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