ClinVar Miner

List of variants in gene JPH2 reported as benign by Labcorp Genetics (formerly Invitae), Labcorp

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Gene type:
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Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_020433.5(JPH2):c.156C>T (p.Tyr52=) rs1883790 0.86681
NM_020433.5(JPH2):c.2073T>C (p.Phe691=) rs6093935 0.33656
NM_020433.5(JPH2):c.1728C>G (p.Pro576=) rs74352869 0.21684
NM_020433.5(JPH2):c.1186G>A (p.Ala396Thr) rs3810510 0.20153
NM_020433.5(JPH2):c.1179C>T (p.His393=) rs7268512 0.08199
NM_020433.5(JPH2):c.1289-7C>T rs116986535 0.02048
NM_020433.5(JPH2):c.1513G>A (p.Gly505Ser) rs140740776 0.01021
NM_020433.5(JPH2):c.661T>C (p.Phe221Leu) rs558770240 0.00596
NM_020433.5(JPH2):c.380-9C>G rs111987307 0.00419
NM_020433.5(JPH2):c.380-6C>T rs201197277 0.00218
NM_020433.5(JPH2):c.562C>T (p.Pro188Ser) rs574746149 0.00214
NM_020433.5(JPH2):c.1794C>A (p.Ser598=) rs369883442 0.00196
NM_020433.5(JPH2):c.637C>T (p.Arg213Trp) rs767328866 0.00145
NM_020433.5(JPH2):c.642G>A (p.Ala214=) rs587780956 0.00128
NM_020433.5(JPH2):c.565G>A (p.Ala189Thr) rs730880254 0.00099
NM_020433.5(JPH2):c.2010+11C>T rs201615229 0.00051
NM_020433.5(JPH2):c.572C>G (p.Pro191Arg) rs554853074 0.00048
NM_020433.5(JPH2):c.1137C>A (p.Ile379=) rs143158930 0.00046
NM_020433.5(JPH2):c.1704C>T (p.Ser568=) rs200892606 0.00046
NM_020433.5(JPH2):c.2011-17C>T rs375414020 0.00042
NM_020433.5(JPH2):c.1410G>A (p.Pro470=) rs751126526 0.00035
NM_020433.5(JPH2):c.780C>T (p.Ala260=) rs199840543 0.00034
NM_020433.5(JPH2):c.1107T>C (p.Ser369=) rs148311735 0.00033
NM_020433.5(JPH2):c.1566G>A (p.Arg522=) rs559143345 0.00031
NM_020433.5(JPH2):c.483G>A (p.Thr161=) rs746384802 0.00023
NM_020433.5(JPH2):c.1731G>A (p.Glu577=) rs530433203 0.00006
NM_020433.5(JPH2):c.379+20C>T rs551866698 0.00003
NM_020433.5(JPH2):c.1185_1186delinsAA (p.Ala396Thr) rs1060503798

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