ClinVar Miner

List of variants in gene PRKG1 reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_006258.4(PRKG1):c.1001+223G>A rs7097336 0.99847
NM_006258.4(PRKG1):c.1313+194T>C rs1194516 0.89799
NM_001098512.3(PRKG1):c.-474C>T rs2248908 0.81301
NM_006258.4(PRKG1):c.762+113C>T rs10823860 0.75789
NM_006258.4(PRKG1):c.762+256C>A rs7083138 0.75786
NM_006258.4(PRKG1):c.762+146G>A rs7081919 0.75582
NM_006258.4(PRKG1):c.1076+31C>A rs10824173 0.74801
NM_006258.4(PRKG1):c.1710-252G>A rs7916242 0.62081
NM_006258.4(PRKG1):c.1962+29G>A rs10762675 0.48091
NM_006258.4(PRKG1):c.*253_*254insG rs5784918 0.48078
NM_006258.4(PRKG1):c.1173+239A>G rs10824300 0.46905
NM_006258.4(PRKG1):c.840+62C>T rs12778630 0.38605
NM_006258.4(PRKG1):c.763-296A>G rs1904008 0.38340
NM_006258.4(PRKG1):c.763-291A>C rs1904009 0.38336
NM_006258.4(PRKG1):c.936-216C>T rs34582712 0.33289
NM_006258.4(PRKG1):c.*157C>T rs1881597 0.27262
NM_006258.4(PRKG1):c.762+274G>T rs34873454 0.27250
NM_006258.4(PRKG1):c.762+132A>G rs11000040 0.20928
NM_006258.4(PRKG1):c.936-61A>T rs17642863 0.16867
NM_006258.4(PRKG1):c.1001+206T>C rs58118931 0.15673
NM_006258.4(PRKG1):c.1896-149G>A rs41281544 0.13456
NM_006258.4(PRKG1):c.936-295C>A rs77138124 0.12074
NM_006258.4(PRKG1):c.1896-263G>A rs16928983 0.11275
NM_001098512.3(PRKG1):c.267-79022C>T rs12264657 0.08789
NM_006258.4(PRKG1):c.479-9C>T rs45615337 0.07983
NM_006258.4(PRKG1):c.1314-195C>T rs16928725 0.07297
NM_006258.4(PRKG1):c.1002-65C>T rs73344945 0.05135
NM_006258.4(PRKG1):c.1008T>C (p.Phe336=) rs56047641 0.04937
NM_006258.4(PRKG1):c.1895+170A>G rs11001464 0.04558
NM_006258.4(PRKG1):c.845A>G (p.Asn282Ser) rs34997494 0.03846
NM_006258.4(PRKG1):c.1173+215T>A rs77530078 0.03816
NM_006258.4(PRKG1):c.935+262C>T rs17560996 0.03775
NM_006258.4(PRKG1):c.936-170G>T rs16927140 0.03308
NM_006258.4(PRKG1):c.1076+125A>C rs7897308 0.03249
NM_006258.4(PRKG1):c.1173+214C>A rs79543394 0.03148
NM_006258.4(PRKG1):c.1076+114G>C rs7908413 0.03026
NM_006258.4(PRKG1):c.312-170del rs75959880 0.02940
NM_006258.4(PRKG1):c.1174-217T>C rs74135384 0.02572
NM_006258.4(PRKG1):c.1403+28A>G rs76977136 0.02474
NM_006258.4(PRKG1):c.1709+178G>A rs16928850 0.02385
NM_006258.4(PRKG1):c.762+104A>T rs74135025 0.02329
NM_001098512.3(PRKG1):c.-359del rs201938144 0.02272
NM_006258.4(PRKG1):c.888T>C (p.Leu296=) rs113994747 0.02057
NM_006258.4(PRKG1):c.936-70T>C rs115286711 0.01810
NM_006258.4(PRKG1):c.408G>A (p.Pro136=) rs55806342 0.01729
NM_006258.4(PRKG1):c.593-192A>C rs16913410 0.01680
NM_006258.4(PRKG1):c.1963-151A>G rs9664313 0.01665
NM_006258.4(PRKG1):c.1080T>C (p.Tyr360=) rs141218982 0.00519
NM_006258.4(PRKG1):c.426C>T (p.Asp142=) rs55754654 0.00405
NM_006258.4(PRKG1):c.-31C>T rs41274080 0.00211
NM_006258.4(PRKG1):c.675C>T (p.Thr225=) rs142166726 0.00124
NM_006258.4(PRKG1):c.1525C>T (p.His509Tyr) rs139646798 0.00109
NM_006258.4(PRKG1):c.840+14G>T rs146372571 0.00025
NC_000010.11:g.50990877del rs111693383
NM_001098512.3(PRKG1):c.-49_-48insTGC rs35361017
NM_001098512.3(PRKG1):c.-68GCC[12] rs79957958
NM_001098512.3(PRKG1):c.-68GCC[15] rs79957958
NM_001098512.3(PRKG1):c.-68GCC[8] rs79957958
NM_006258.4(PRKG1):c.1076+19_1076+20insTGGCCTT rs146504019
NM_006258.4(PRKG1):c.1174-84G>T rs10454466
NM_006258.4(PRKG1):c.1545+27G>T rs7912782
NM_006258.4(PRKG1):c.312-170G>T rs3740292
NM_006258.4(PRKG1):c.478+163_478+166del rs142371458
NM_006258.4(PRKG1):c.699-118del rs34697221
NM_006258.4(PRKG1):c.699-118dup rs34697221
NM_006258.4(PRKG1):c.763-15G>T rs1904010

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