ClinVar Miner

List of variants in gene ARHGEF9 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 42
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HGVS dbSNP gnomAD frequency
NM_001353921.2(ARHGEF9):c.1078-324C>A rs113913751 0.01045
NM_001353921.2(ARHGEF9):c.815+302C>T rs111561520 0.01015
NM_001353921.2(ARHGEF9):c.1390+163C>T rs141945280 0.00877
NM_001353921.2(ARHGEF9):c.815+175T>C rs138067049 0.00781
NM_001353921.2(ARHGEF9):c.*7C>G rs202232026 0.00027
NM_001353921.2(ARHGEF9):c.939C>G (p.Asp313Glu) rs143490560 0.00025
NM_001353921.2(ARHGEF9):c.946-4C>A rs56398019 0.00020
NM_001353921.2(ARHGEF9):c.579G>A (p.Glu193=) rs56182751 0.00016
NM_001353921.2(ARHGEF9):c.885G>A (p.Lys295=) rs199625034 0.00016
NM_001353921.2(ARHGEF9):c.1471G>A (p.Asp491Asn) rs782577519 0.00015
NM_001353921.2(ARHGEF9):c.1488G>A (p.Ser496=) rs782580975 0.00015
NM_001353921.2(ARHGEF9):c.946-16C>T rs781867369 0.00011
NM_001353921.2(ARHGEF9):c.1386A>G (p.Gln462=) rs782354481 0.00009
NM_001353921.2(ARHGEF9):c.31-29583C>A rs370045250 0.00009
NM_001353921.2(ARHGEF9):c.582C>T (p.His194=) rs150129110 0.00008
NM_001353921.2(ARHGEF9):c.24G>A (p.Ser8=) rs1413001108 0.00007
NM_001353921.2(ARHGEF9):c.351G>A (p.Glu117=) rs373866956 0.00006
NM_001353921.2(ARHGEF9):c.777G>A (p.Gln259=) rs1057522740 0.00006
NM_001353921.2(ARHGEF9):c.747A>C (p.Pro249=) rs369716500 0.00005
NM_001353921.2(ARHGEF9):c.372C>T (p.His124=) rs138198839 0.00004
NM_001353921.2(ARHGEF9):c.564A>T (p.Gly188=) rs782187939 0.00003
NM_001353921.2(ARHGEF9):c.583-18T>G rs1057521815 0.00003
NM_001353921.2(ARHGEF9):c.1322-31A>G rs576608472 0.00002
NM_001353921.2(ARHGEF9):c.31-29639A>T rs782573720 0.00002
NM_001353921.2(ARHGEF9):c.1218T>A (p.Thr406=) rs1057521807 0.00001
NM_001353921.2(ARHGEF9):c.1506C>T (p.Thr502=) rs782129771 0.00001
NM_001353921.2(ARHGEF9):c.252C>T (p.Ser84=) rs1367866917 0.00001
NM_001353921.2(ARHGEF9):c.289T>C (p.Cys97Arg) rs1057524386 0.00001
NM_001353921.2(ARHGEF9):c.1078-18C>T rs781901799
NM_001353921.2(ARHGEF9):c.1322-120del rs35995120
NM_001353921.2(ARHGEF9):c.1390+262del rs560889265
NM_001353921.2(ARHGEF9):c.1546A>G (p.Ser516Gly) rs2047402332
NM_001353921.2(ARHGEF9):c.234G>A (p.Glu78=) rs868932053
NM_001353921.2(ARHGEF9):c.31-29642del rs782757577
NM_001353921.2(ARHGEF9):c.561A>T (p.Ile187=) rs1057522301
NM_001353921.2(ARHGEF9):c.583-11dup rs782366734
NM_001353921.2(ARHGEF9):c.583-296del rs200948030
NM_001353921.2(ARHGEF9):c.726C>A (p.Ile242=) rs1556365224
NM_001353921.2(ARHGEF9):c.816-12_816-11del rs781845457
NM_001353921.2(ARHGEF9):c.816-9T>C rs1057522347
NM_001353921.2(ARHGEF9):c.946-333AG[13] rs368308422
NM_001353921.2(ARHGEF9):c.948C>A (p.Gly316=) rs141158169

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