ClinVar Miner

List of variants in gene PRPH2 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_000322.5(PRPH2):c.929G>A (p.Arg310Lys) rs425876 0.92861
NM_000322.5(PRPH2):c.829-261G>T rs415906 0.77340
NM_000322.5(PRPH2):c.*1375C>T rs405043 0.77180
NM_000322.5(PRPH2):c.*1357C>T rs405059 0.77171
NM_000322.5(PRPH2):c.*543G>A rs432753 0.77168
NM_000322.5(PRPH2):c.*762C>T rs1758213 0.77165
NC_000006.12:g.42722950A>C rs9381213 0.59764
NM_000322.5(PRPH2):c.582-67T>A rs3818086 0.56178
NM_000322.5(PRPH2):c.581+81C>T rs6928781 0.32828
NC_000006.12:g.42722776G>A rs11754813 0.32278
NM_000322.5(PRPH2):c.582-225C>T rs13214506 0.25566
NM_000322.5(PRPH2):c.582-85G>A rs34722725 0.25301
NM_000322.5(PRPH2):c.828+241del rs67162942 0.25118
NM_000322.5(PRPH2):c.582-58A>G rs3818087 0.24683
NM_000322.5(PRPH2):c.*145G>A rs835 0.24219
NM_000322.5(PRPH2):c.*898C>A rs3176988 0.22759
NM_000322.5(PRPH2):c.*1001C>A rs45550933 0.22757
NM_000322.5(PRPH2):c.829-48C>T rs41273820 0.22114
NM_000322.5(PRPH2):c.828+244T>A rs555942731 0.07839
NM_000322.5(PRPH2):c.*132C>T rs77363417 0.02609
NM_000322.5(PRPH2):c.*174C>T rs73426412 0.02603
NM_000322.5(PRPH2):c.*276G>C rs76754927 0.02448
NM_000322.5(PRPH2):c.*1370A>T rs1804284 0.02154
NM_000322.5(PRPH2):c.*839G>A rs73426405 0.02142
NM_000322.5(PRPH2):c.*1565G>A rs41273818 0.00908
NM_000322.4:c.+13C>T
NM_000322.5(PRPH2):c.*483_*484dup rs55851577
NM_000322.5(PRPH2):c.*484del rs55851577
NM_000322.5(PRPH2):c.483C>T (p.Ile161=) rs76989855
NM_000322.5(PRPH2):c.828+176TATT[5] rs59389246
NM_000322.5(PRPH2):c.828+176TATT[7] rs59389246
NM_000322.5(PRPH2):c.828+260del rs58317577
NM_000322.5(PRPH2):c.828+284_828+285del rs67449353
NM_000322.5(PRPH2):c.829-120C>G rs389999
NM_000322.5(PRPH2):c.829-230A>G rs433286

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