ClinVar Miner

List of variants in gene GPD1L reported as likely benign by GeneDx

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Gene type:
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Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_015141.4(GPD1L):c.506-124C>G rs72558072 0.01959
NM_015141.3(GPD1L):c.*132T>C rs147700828 0.01748
NM_015141.4(GPD1L):c.506-79C>T rs9839561 0.01394
NM_015141.4(GPD1L):c.226-42G>C rs116185919 0.01392
NM_015141.4(GPD1L):c.853-41T>G rs72546641 0.01124
NM_015141.4(GPD1L):c.959+71C>T rs66691298 0.00819
NM_015141.4(GPD1L):c.506-290C>T rs144267030 0.00584
NM_015141.4(GPD1L):c.*171T>G rs114506248 0.00523
NM_015141.3(GPD1L):c.-365G>A rs573499355 0.00378
NM_015141.4(GPD1L):c.370A>G (p.Ile124Val) rs72552293 0.00291
NM_015141.4(GPD1L):c.659G>A (p.Arg220His) rs72546648 0.00130
NM_015141.4(GPD1L):c.619-28C>T rs534799892 0.00097
NM_015141.4(GPD1L):c.619-9C>G rs2044880 0.00057
NM_015141.4(GPD1L):c.828C>T (p.Ala276=) rs200392121 0.00055
NM_015141.4(GPD1L):c.813G>T (p.Arg271=) rs35464343 0.00031
NM_015141.4(GPD1L):c.459C>T (p.Asn153=) rs375532052 0.00019
NM_015141.4(GPD1L):c.*16G>A rs372500383 0.00018
NM_015141.4(GPD1L):c.1038C>T (p.Ser346=) rs147092668 0.00016
NM_015141.4(GPD1L):c.445C>T (p.Leu149=) rs146738300 0.00015
NM_015141.4(GPD1L):c.837C>T (p.Phe279=) rs376724853 0.00013
NM_015141.4(GPD1L):c.959+11C>T rs370985609 0.00011
NM_015141.4(GPD1L):c.897C>T (p.Leu299=) rs192905901 0.00009
NM_015141.4(GPD1L):c.906G>A (p.Pro302=) rs200045526 0.00009
NM_015141.4(GPD1L):c.996C>T (p.Tyr332=) rs149423659 0.00006
NM_015141.4(GPD1L):c.774C>T (p.Cys258=) rs753955088 0.00002
NM_015141.4(GPD1L):c.384C>T (p.Pro128=) rs779990114 0.00001
NM_015141.4(GPD1L):c.684C>T (p.Ala228=) rs545047908 0.00001
NM_015141.4(GPD1L):c.852+20C>T rs189819292 0.00001
NM_015141.4(GPD1L):c.336C>A (p.Pro112=) rs1553659667
NM_015141.4(GPD1L):c.48-6_48-3dup rs1553658254
NM_015141.4(GPD1L):c.505+292_505+319del rs143613693
NM_015141.4(GPD1L):c.506-342G>A rs79282795
NM_015141.4(GPD1L):c.618+17G>C rs775325609
NM_015141.4(GPD1L):c.853-22T>C rs530148424
NM_015141.4(GPD1L):c.959+7C>A rs1057523126

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