ClinVar Miner

List of variants in gene RIN2 reported as uncertain significance by GeneDx

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Total variants: 49
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HGVS dbSNP gnomAD frequency
NM_018993.4(RIN2):c.2501A>T (p.Tyr834Phe) rs183141566 0.00108
NM_018993.4(RIN2):c.2627T>C (p.Ile876Thr) rs202076384 0.00077
NM_018993.4(RIN2):c.2657A>G (p.Gln886Arg) rs529654225 0.00053
NM_018993.4(RIN2):c.604G>A (p.Glu202Lys) rs200682836 0.00043
NM_018993.4(RIN2):c.41G>A (p.Arg14Gln) rs367797077 0.00032
NM_018993.4(RIN2):c.797A>T (p.Asn266Ile) rs201551000 0.00030
NM_018993.4(RIN2):c.2398A>T (p.Ser800Cys) rs368984007 0.00021
NM_018993.4(RIN2):c.995C>A (p.Thr332Lys) rs180981486 0.00019
NM_018993.4(RIN2):c.2673C>A (p.Asp891Glu) rs759973625 0.00011
NM_018993.4(RIN2):c.590C>T (p.Ser197Leu) rs531782187 0.00011
NM_018993.4(RIN2):c.98A>G (p.Gln33Arg) rs370464072 0.00011
NM_018993.4(RIN2):c.217C>T (p.Arg73Trp) rs372531454 0.00009
NM_018993.4(RIN2):c.2637T>A (p.Asp879Glu) rs368180718 0.00009
NM_018993.4(RIN2):c.403C>T (p.Arg135Cys) rs201981815 0.00009
NM_018993.4(RIN2):c.508C>T (p.Arg170Trp) rs377681843 0.00006
NM_018993.4(RIN2):c.1344G>C (p.Met448Ile) rs781480608 0.00004
NM_018993.4(RIN2):c.548C>T (p.Pro183Leu) rs201491053 0.00004
NM_018993.4(RIN2):c.922C>G (p.Pro308Ala) rs61743185 0.00004
NM_018993.4(RIN2):c.2320C>T (p.Arg774Trp) rs772994328 0.00003
NM_018993.4(RIN2):c.586A>C (p.Lys196Gln) rs1057087286 0.00003
NM_018993.4(RIN2):c.235A>G (p.Ser79Gly) rs751979478 0.00002
NM_018993.4(RIN2):c.1334A>G (p.Asp445Gly) rs1337320171 0.00001
NM_018993.4(RIN2):c.1408C>G (p.Gln470Glu) rs752982932 0.00001
NM_018993.4(RIN2):c.1472A>G (p.Lys491Arg) rs773174079 0.00001
NM_018993.4(RIN2):c.1904A>G (p.Asn635Ser) rs767135541 0.00001
NM_018993.4(RIN2):c.2091C>A (p.Asp697Glu) rs188766763 0.00001
NM_018993.4(RIN2):c.2192A>G (p.His731Arg) rs990323695 0.00001
NM_018993.4(RIN2):c.685C>T (p.Pro229Ser) rs1357960211 0.00001
NM_018993.4(RIN2):c.935C>A (p.Pro312Gln) rs368837181 0.00001
NM_018993.4(RIN2):c.1219G>T (p.Asp407Tyr)
NM_018993.4(RIN2):c.1258C>G (p.Pro420Ala)
NM_018993.4(RIN2):c.1819G>A (p.Val607Met) rs575189955
NM_018993.4(RIN2):c.1972T>C (p.Phe658Leu)
NM_018993.4(RIN2):c.2000C>A (p.Pro667Gln) rs371995628
NM_018993.4(RIN2):c.2260G>A (p.Glu754Lys) rs375974979
NM_018993.4(RIN2):c.2396del (p.Asn799fs) rs2146439245
NM_018993.4(RIN2):c.2431C>A (p.Pro811Thr) rs1408690708
NM_018993.4(RIN2):c.247A>G (p.Arg83Gly) rs375970512
NM_018993.4(RIN2):c.249G>C (p.Arg83Ser) rs769359621
NM_018993.4(RIN2):c.2521G>A (p.Asp841Asn) rs2146439961
NM_018993.4(RIN2):c.2635G>A (p.Asp879Asn)
NM_018993.4(RIN2):c.2650A>G (p.Ile884Val)
NM_018993.4(RIN2):c.277A>G (p.Thr93Ala) rs1555800471
NM_018993.4(RIN2):c.338C>A (p.Ala113Asp) rs1131691814
NM_018993.4(RIN2):c.344C>T (p.Pro115Leu) rs2146237832
NM_018993.4(RIN2):c.447A>G (p.Ile149Met) rs1057524446
NM_018993.4(RIN2):c.680A>G (p.His227Arg)
NM_018993.4(RIN2):c.799G>C (p.Gly267Arg)
NM_018993.4(RIN2):c.923C>T (p.Pro308Leu) rs374058245

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