ClinVar Miner

List of variants in gene RIN2 reported as benign for not provided

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Gene type:
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Total variants: 68
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HGVS dbSNP gnomAD frequency
NM_018993.4(RIN2):c.-36-225T>C rs2208448 0.51417
NM_018993.4(RIN2):c.1818C>T (p.His606=) rs2076584 0.35224
NM_018993.4(RIN2):c.463+83A>T rs199562 0.30904
NM_018993.4(RIN2):c.2068+157G>A rs199604 0.27471
NM_018993.4(RIN2):c.-36-3168C>T rs6132239 0.24831
NM_018993.4(RIN2):c.352-313G>A rs3748485 0.21319
NM_018993.4(RIN2):c.628+87C>T rs3803982 0.20735
NM_018993.4(RIN2):c.464-103T>C rs6046489 0.16201
NM_018993.4(RIN2):c.628+289C>T rs2273103 0.15418
NM_018993.4(RIN2):c.589T>A (p.Ser197Thr) rs3803981 0.15165
NM_018993.4(RIN2):c.2201-47G>A rs6136905 0.10785
NM_018993.4(RIN2):c.158+301T>C rs16981333 0.09192
NM_018993.4(RIN2):c.2001G>A (p.Pro667=) rs35151304 0.06850
NM_018993.4(RIN2):c.58-65C>G rs117184213 0.04084
NM_018993.4(RIN2):c.-36-3284G>A rs75113125 0.03726
NM_018993.4(RIN2):c.212G>A (p.Cys71Tyr) rs142502440 0.03307
NM_018993.4(RIN2):c.1762+167G>A rs78976197 0.03276
NM_018993.4(RIN2):c.-36-2484G>A rs73277492 0.02944
NM_018993.4(RIN2):c.628+249G>A rs7265887 0.02603
NM_018993.4(RIN2):c.-11C>T rs56311184 0.02573
NM_018993.4(RIN2):c.375C>T (p.Thr125=) rs45481396 0.02341
NM_018993.4(RIN2):c.1044G>C (p.Leu348=) rs149398614 0.02129
NM_018993.4(RIN2):c.-36-2804C>A rs73901320 0.02028
NM_018993.4(RIN2):c.-36-2954C>T rs6112633 0.01667
NM_018993.4(RIN2):c.-36-2957del rs11476169 0.01559
NM_018993.4(RIN2):c.804C>T (p.Ala268=) rs41306763 0.01538
NM_018993.4(RIN2):c.-36-230G>A rs77407125 0.01513
NM_018993.4(RIN2):c.85G>A (p.Gly29Arg) rs78648341 0.01238
NM_018993.4(RIN2):c.427C>T (p.Pro143Ser) rs45488002 0.00966
NM_018993.4(RIN2):c.2068+32G>A rs138759147 0.00712
NM_018993.4(RIN2):c.84C>T (p.Ile28=) rs181853315 0.00670
NM_018993.4(RIN2):c.1927G>A (p.Ala643Thr) rs199603 0.00643
NM_018993.4(RIN2):c.629-19C>T rs77182595 0.00592
NM_018993.4(RIN2):c.965G>A (p.Ser322Asn) rs199693970 0.00538
NM_018993.4(RIN2):c.347C>T (p.Pro116Leu) rs147968123 0.00335
NM_018993.4(RIN2):c.2069-8G>A rs78124032 0.00329
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.604G>A (p.Glu202Lys) rs200682836 0.00043
NM_018993.4(RIN2):c.2027G>A (p.Arg676Gln) rs567590350 0.00029
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.2355C>T (p.Asp785=) rs186967436 0.00014
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.57+23A>T rs377683961 0.00005
NM_018993.4(RIN2):c.-36-2528del rs377364690
NM_018993.4(RIN2):c.-36-2865del rs72242041
NM_018993.4(RIN2):c.-36-2935del rs11362637
NM_018993.4(RIN2):c.-36-2935dup rs11362637
NM_018993.4(RIN2):c.1642G>A (p.Val548Met) rs181298473
NM_018993.4(RIN2):c.258C>A (p.Ile86=)
NM_018993.4(RIN2):c.536+197G>T rs1106817
NM_018993.4(RIN2):c.628+268dup rs11461198

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