ClinVar Miner

List of variants reported as association for carcinoma

Included ClinVar conditions (243):
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ClinVar version:
Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_170672.3(RASGRP3):c.-261+9727G>T rs2124437 0.65924
NM_015589.6(SAMD4A):c.1176+4220T>C rs1957358 0.47434
NM_024870.4(PREX2):c.142-2489C>T rs4512367 0.44051
NM_021021.4(SNTB1):c.571+12964G>A rs10090787 0.34456
NM_021956.5(GRIK2):c.2086-16819C>T rs1335022 0.26908
NM_175607.3(CNTN4):c.55+61947C>T rs9849237 0.25236
NM_004996.4(ABCC1):c.2461-1217G>A rs3888565 0.25007
NM_004530.5(MMP2):c.-1586C>T rs243865 0.18794
NM_004996.4(ABCC1):c.1988+848A>G rs35628 0.12670
NM_032217.5(ANKRD17):c.7731G>A (p.Thr2577=) rs2306058 0.12670
NM_002012.4(FHIT):c.104-196657C>A rs11130760 0.11483
NM_004996.4(ABCC1):c.1988+890G>T rs4148353 0.10946
NM_003981.4(PRC1):c.1462-1016G>A rs11852999 0.10280
NM_003981.4(PRC1):c.971-442C>T rs10520699 0.08779
NC_000008.11:g.127325028_127325029dup rs201361304 0.02419
NC_000008.11:g.127193633G>T rs1428102803 0.00491
NR_109833.1(PRNCR1):n.11999A>G rs183373024 0.00457
NC_000008.11:g.126929548G>A rs182352457 0.00421
NC_000008.11:g.127196124A>G rs138042437 0.00408
NC_000008.11:g.127179427T>A rs188140481 0.00399
NC_000008.11:g.127467731T>C rs78311688 0.00362
NM_024675.4(PALB2):c.2897T>C (p.Ile966Thr) rs587780214 0.00003
NC_000008.11:g.127273164ATAA[1] rs201885483
NM_000314.8(PTEN):c.332G>A (p.Trp111Ter)
NM_005591.4(MRE11):c.901C>G (p.Leu301Val) rs863225441
NM_006015.6(ARID1A):c.6436_6438del (p.Lys2146del)
NM_006297.3(XRCC1):c.*13AC[12]
NM_006297.3(XRCC1):c.*13AC[17]
NM_006297.3(XRCC1):c.602-33C>T
NM_006297.3(XRCC1):c.839G>A (p.Arg280His)
NM_007194.4(CHEK2):c.1085G>A (p.Cys362Tyr) rs767306337
chr10:108525702..109883836 complex variant
chr12:13090968..16310672 complex variant
chr14:20635208..21155433 complex variant

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