ClinVar Miner

Variants in gene RIN2 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 25
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HGVS dbSNP gnomAD frequency
NM_018993.4(RIN2):c.84C>T (p.Ile28=) rs181853315 0.00670
NM_018993.4(RIN2):c.965G>A (p.Ser322Asn) rs199693970 0.00538
NM_018993.4(RIN2):c.1425C>A (p.Pro475=) rs188147644 0.00315
NM_018993.4(RIN2):c.2571G>A (p.Lys857=) rs149821491 0.00295
NM_018993.4(RIN2):c.1141C>T (p.Arg381Trp) rs199954296 0.00249
NM_018993.4(RIN2):c.1338G>C (p.Arg446=) rs367993633 0.00243
NM_018993.4(RIN2):c.1917G>A (p.Leu639=) rs368610064 0.00239
NM_018993.4(RIN2):c.57+18T>C rs140679811 0.00235
NM_018993.4(RIN2):c.463+12T>C rs184313079 0.00228
NM_018993.4(RIN2):c.2418C>A (p.Thr806=) rs114329888 0.00218
NM_018993.4(RIN2):c.365A>G (p.His122Arg) rs201529870 0.00200
NM_018993.4(RIN2):c.1851C>T (p.Ala617=) rs180817901 0.00173
NM_018993.4(RIN2):c.1427C>G (p.Pro476Arg) rs35142632 0.00165
NM_018993.4(RIN2):c.2220C>T (p.Ser740=) rs146810222 0.00083
NM_018993.4(RIN2):c.1557C>T (p.Ala519=) rs372947881 0.00076
NM_018993.4(RIN2):c.868C>A (p.Arg290=) rs373060422 0.00025
NM_018993.4(RIN2):c.1464G>A (p.Val488=) rs144752607 0.00021
NM_018993.4(RIN2):c.1158G>C (p.Pro386=) rs548499908 0.00016
NM_018993.4(RIN2):c.629-8A>C rs190569230 0.00015
NM_018993.4(RIN2):c.628+7G>A rs370585631 0.00010
NM_018993.4(RIN2):c.1239G>T (p.Pro413=) rs534193230 0.00009
NM_018993.4(RIN2):c.78G>A (p.Ser26=) rs377404678 0.00009
NM_018993.4(RIN2):c.2436C>T (p.Tyr812=) rs540923982 0.00007
NM_018993.4(RIN2):c.1642G>A (p.Val548Met) rs181298473
NM_018993.4(RIN2):c.924A>C (p.Pro308=) rs1348842250

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