ClinVar Miner

List of variants in gene PKD2 reported as likely benign for not provided

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Gene type:
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Total variants: 36
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HGVS dbSNP gnomAD frequency
NM_000297.4(PKD2):c.709+300G>T rs76951105 0.03913
NM_000297.4(PKD2):c.596-281C>T rs858 0.01827
NM_000297.4(PKD2):c.1320-196A>T rs77991231 0.01516
NM_000297.4(PKD2):c.1548+242T>C rs76491349 0.01513
NM_000297.4(PKD2):c.2358+288T>A rs188453003 0.01148
NM_000297.4(PKD2):c.2358+290A>G rs192262797 0.01147
NM_000297.4(PKD2):c.710-29G>A rs72873478 0.01046
NM_000297.4(PKD2):c.2358+23G>A rs10516804 0.01042
NM_000297.4(PKD2):c.1359A>G (p.Pro453=) rs17013754 0.00985
NM_000297.4(PKD2):c.1549-117G>C rs79352425 0.00965
NM_000297.4(PKD2):c.2134T>C (p.Leu712=) rs73841280 0.00563
NM_000297.4(PKD2):c.2119-35T>C rs78885971 0.00524
NM_000297.4(PKD2):c.843+116A>G rs114532947 0.00499
NM_000297.4(PKD2):c.2240+114C>T rs1282890679 0.00381
NM_000297.4(PKD2):c.1319+158G>A rs192899890 0.00332
NM_000297.4(PKD2):c.2420G>A (p.Arg807Gln) rs147654263 0.00312
NM_000297.4(PKD2):c.2359-196A>C rs144707808 0.00289
NM_000297.4(PKD2):c.1445T>G (p.Phe482Cys) rs75762896 0.00176
NM_000297.4(PKD2):c.1830G>A (p.Ala610=) rs144968710 0.00091
NM_000297.4(PKD2):c.1836T>C (p.Ala612=) rs145952917 0.00048
NM_000297.4(PKD2):c.1617G>C (p.Leu539=) rs145297759 0.00044
NM_000297.4(PKD2):c.595+15C>T rs559555727 0.00026
NM_000297.4(PKD2):c.994T>G (p.Ser332Ala) rs200314088 0.00013
NM_000297.4(PKD2):c.2523-7C>T rs199528409 0.00011
NM_000297.4(PKD2):c.2214T>C (p.Phe738=) rs772819278 0.00002
NM_000297.4(PKD2):c.2295T>C (p.Asp765=) rs138982773 0.00001
NM_000297.4(PKD2):c.2668G>A (p.Glu890Lys) rs770609334 0.00001
NM_000297.4(PKD2):c.621G>A (p.Glu207=) rs769630264 0.00001
NC_000004.12:g.88007383G>C rs9994525
NM_000297.4(PKD2):c.*235dup rs200938134
NM_000297.4(PKD2):c.1587A>T (p.Thr529=) rs375543446
NM_000297.4(PKD2):c.1717-33C>T
NM_000297.4(PKD2):c.2020-158dup rs60055635
NM_000297.4(PKD2):c.2164G>T (p.Val722Leu) rs529945469
NM_000297.4(PKD2):c.2670+27G>A
NM_000297.4(PKD2):c.596-116dup rs200521275

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