ClinVar Miner

List of variants in gene ABCC9 reported as benign for not provided

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Gene type:
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Total variants: 41
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HGVS dbSNP
NC_000012.12:g.21845349_21845350del
NC_000012.12:g.21852069T>G
NM_005691.3(ABCC9):c.1012-276A>G
NM_005691.3(ABCC9):c.1056C>T (p.Tyr352=) rs149408382
NM_005691.3(ABCC9):c.1164+85T>A
NM_005691.3(ABCC9):c.1321-287A>G
NM_005691.3(ABCC9):c.143-301A>G
NM_005691.3(ABCC9):c.1803-188_1803-177del
NM_005691.3(ABCC9):c.1912-234T>C
NM_005691.3(ABCC9):c.1912-66G>A
NM_005691.3(ABCC9):c.2019+275T>C
NM_005691.3(ABCC9):c.2200G>A (p.Val734Ile) rs61688134
NM_005691.3(ABCC9):c.2237+216C>G
NM_005691.3(ABCC9):c.2238-274_2238-229del
NM_005691.3(ABCC9):c.2339+119C>T
NM_005691.3(ABCC9):c.2340-233A>G
NM_005691.3(ABCC9):c.2506-332T>C
NM_005691.3(ABCC9):c.2643+44C>A
NM_005691.3(ABCC9):c.2769+194del
NM_005691.3(ABCC9):c.2770-192C>T
NM_005691.3(ABCC9):c.285-266A>G
NM_005691.3(ABCC9):c.285-321C>T
NM_005691.3(ABCC9):c.2867-342A>C
NM_005691.3(ABCC9):c.3315+296C>G
NM_005691.3(ABCC9):c.3409G>A (p.Val1137Ile) rs147895473
NM_005691.3(ABCC9):c.3473+216T>C
NM_005691.3(ABCC9):c.3473+293C>G
NM_005691.3(ABCC9):c.3567-287T>C
NM_005691.3(ABCC9):c.3567-333T>C
NM_005691.3(ABCC9):c.3670-94G>T
NM_005691.3(ABCC9):c.3892+102G>A
NM_005691.3(ABCC9):c.3892+224C>T
NM_005691.3(ABCC9):c.406+305A>T
NM_005691.3(ABCC9):c.406+320A>G
NM_005691.3(ABCC9):c.407-194A>G
NM_005691.3(ABCC9):c.4103-79A>G
NM_005691.3(ABCC9):c.4212-129G>T
NM_005691.3(ABCC9):c.4449+204C>T
NM_005691.3(ABCC9):c.4513-154C>G
NM_005691.3(ABCC9):c.574-270C>A
NM_005691.3(ABCC9):c.817-180G>A

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