ClinVar Miner

List of variants in gene FOLR1 reported by GeneDx

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Gene type:
ClinVar version:
Total variants: 68
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HGVS dbSNP gnomAD frequency
NC_000011.10:g.72196438T>C rs68068983 0.10633
NM_016729.3(FOLR1):c.169-186C>G rs35805771 0.10537
NC_000011.10:g.72196454C>T rs34030891 0.06606
NM_016729.3(FOLR1):c.169-71T>C rs17162056 0.04211
NM_000802.3(FOLR1):c.-9+870A>C rs7125189 0.04036
NM_000802.3(FOLR1):c.-9+695C>T rs7109250 0.03781
NM_000802.3(FOLR1):c.-9+516G>A rs1540087 0.03757
NM_000802.3(FOLR1):c.-9+153G>A rs117787264 0.03562
NM_000802.3(FOLR1):c.-9+603C>T rs9282688 0.02591
NM_016729.3(FOLR1):c.168+46G>C rs77405781 0.01933
NM_016729.3(FOLR1):c.169-94T>G rs74702497 0.01680
NM_016729.3(FOLR1):c.168+37G>T rs77771906 0.01233
NM_016729.3(FOLR1):c.292C>T (p.Arg98Trp) rs76191655 0.00274
NM_016729.3(FOLR1):c.508G>A (p.Ala170Thr) rs139633601 0.00172
NM_016729.3(FOLR1):c.493+2T>C rs144637717 0.00134
NM_016729.3(FOLR1):c.321C>T (p.Tyr107=) rs145674759 0.00052
NM_016729.3(FOLR1):c.396G>A (p.Val132=) rs35179028 0.00033
NM_016729.3(FOLR1):c.157T>C (p.Leu53=) rs143413500 0.00029
NM_016729.3(FOLR1):c.103A>G (p.Asn35Asp) rs149216939 0.00028
NM_016729.3(FOLR1):c.117C>T (p.Asn39=) rs376392205 0.00026
NM_016725.3(FOLR1):c.-30G>A rs919336828 0.00018
NM_016729.3(FOLR1):c.357+8T>A rs886042924 0.00016
NM_016729.3(FOLR1):c.357+18C>A rs754798966 0.00015
NM_016729.3(FOLR1):c.-14C>T rs375060832 0.00010
NM_016729.3(FOLR1):c.719C>T (p.Ala240Val) rs147155003 0.00010
NM_016729.3(FOLR1):c.215A>G (p.Gln72Arg) rs148345688 0.00006
NM_016729.3(FOLR1):c.677C>T (p.Ala226Val) rs371399726 0.00006
NM_016729.3(FOLR1):c.391A>G (p.Asn131Asp) rs1029995293 0.00005
NM_016729.3(FOLR1):c.13A>G (p.Met5Val) rs371565364 0.00004
NM_016729.3(FOLR1):c.373C>T (p.Arg125Cys) rs752503322 0.00004
NM_016729.3(FOLR1):c.724T>A (p.Trp242Arg) rs796052445 0.00003
NM_016729.3(FOLR1):c.447C>T (p.Ser149=) rs191657981 0.00002
NM_016729.3(FOLR1):c.493+12G>A rs190090266 0.00002
NM_016729.3(FOLR1):c.163G>A (p.Glu55Lys) rs1370692247 0.00001
NM_016729.3(FOLR1):c.168+13G>A rs745859325 0.00001
NM_016729.3(FOLR1):c.261C>T (p.Asn87=) rs375444839 0.00001
NM_016729.3(FOLR1):c.281C>G (p.Pro94Arg) rs759712157 0.00001
NM_016729.3(FOLR1):c.333C>T (p.Pro111=) rs772210412 0.00001
NM_016729.3(FOLR1):c.358-2A>G rs369395654 0.00001
NM_016729.3(FOLR1):c.45G>T (p.Trp15Cys) rs200261943 0.00001
NM_016729.3(FOLR1):c.57A>G (p.Val19=) rs769589754 0.00001
NM_016729.3(FOLR1):c.588C>T (p.Ser196=) rs755278391 0.00001
NM_016729.3(FOLR1):c.9G>A (p.Gln3=) rs1555068614 0.00001
NM_000802.3(FOLR1):c.-20G>A rs2071010
NM_016725.3(FOLR1):c.-9+9C>T rs1057522827
NM_016729.3(FOLR1):c.111C>T (p.Cys37=) rs997052303
NM_016729.3(FOLR1):c.11G>A (p.Arg4Gln) rs145380453
NM_016729.3(FOLR1):c.124C>A (p.His42Asn) rs754414177
NM_016729.3(FOLR1):c.168+9G>A rs1555068677
NM_016729.3(FOLR1):c.190G>T (p.Ala64Ser) rs1131691637
NM_016729.3(FOLR1):c.192C>T (p.Ala64=) rs1057523002
NM_016729.3(FOLR1):c.1A>G (p.Met1Val) rs1057524829
NM_016729.3(FOLR1):c.227del (p.Lys76fs)
NM_016729.3(FOLR1):c.237C>T (p.Ser79=) rs867175310
NM_016729.3(FOLR1):c.317T>C (p.Leu106Pro)
NM_016729.3(FOLR1):c.322G>A (p.Glu108Lys) rs1555069113
NM_016729.3(FOLR1):c.357+1G>A rs1057518027
NM_016729.3(FOLR1):c.358-18T>A rs1057521333
NM_016729.3(FOLR1):c.412G>A (p.Asp138Asn) rs796052442
NM_016729.3(FOLR1):c.489T>C (p.Thr163=) rs796052440
NM_016729.3(FOLR1):c.493+20G>A rs1555069209
NM_016729.3(FOLR1):c.493G>T (p.Gly165Trp) rs913171756
NM_016729.3(FOLR1):c.510A>G (p.Ala170=) rs564331848
NM_016729.3(FOLR1):c.59G>C (p.Gly20Ala) rs566120497
NM_016729.3(FOLR1):c.610C>T (p.Arg204Ter) rs952165627
NM_016729.3(FOLR1):c.694G>A (p.Ala232Thr) rs796052443
NM_016729.3(FOLR1):c.714C>T (p.Pro238=) rs1057520942
NM_016729.3(FOLR1):c.81A>C (p.Ala27=) rs1057520285

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