ClinVar Miner

List of variants in gene CD36 reported as uncertain significance for hematologic disorder

Included ClinVar conditions (819):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 90
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HGVS dbSNP gnomAD frequency
NM_001001548.3(CD36):c.975T>G (p.Tyr325Ter) rs3211938 0.02669
NM_001001548.3(CD36):c.573G>A (p.Pro191=) rs5956 0.01947
NM_001001548.3(CD36):c.*1419+226A>G rs8956 0.01157
NM_001001548.3(CD36):c.*1419+202G>T rs143304806 0.00443
NM_001001548.3(CD36):c.429+2T>C rs3211893 0.00220
NM_001001547.3(CD36):c.-287G>A rs190767214 0.00213
NM_001001548.3(CD36):c.591A>T (p.Thr197=) rs141680676 0.00150
NM_001001547.3(CD36):c.-193C>G rs182279912 0.00076
NM_001001548.3(CD36):c.879T>C (p.Phe293=) rs188717259 0.00066
NM_001001548.3(CD36):c.1133G>T (p.Gly378Val) rs146027667 0.00060
NM_001001548.3(CD36):c.1404G>A (p.Ser468=) rs141626483 0.00055
NM_001001548.3(CD36):c.390A>T (p.Thr130=) rs148114593 0.00047
NM_001001548.3(CD36):c.1163A>T (p.Gln388Leu) rs201355711 0.00041
NM_001001548.3(CD36):c.550G>A (p.Asp184Asn) rs138897347 0.00034
NM_001001548.3(CD36):c.*1419+163C>T rs531464767 0.00026
NM_001001548.3(CD36):c.572C>T (p.Pro191Leu) rs143150225 0.00026
NM_001001547.3(CD36):c.-211C>T rs151218598 0.00024
NM_001001548.3(CD36):c.655G>T (p.Asp219Tyr) rs201715989 0.00024
NM_001001548.3(CD36):c.649G>A (p.Gly217Arg) rs200067322 0.00023
NM_001001548.3(CD36):c.5G>T (p.Gly2Val) rs201759988 0.00020
NM_001001548.3(CD36):c.1079T>G (p.Leu360Ter) rs56381858 0.00017
NM_001001548.3(CD36):c.403T>C (p.Phe135Leu) rs140968958 0.00017
NM_001001548.3(CD36):c.1000A>G (p.Lys334Glu) rs199628571 0.00016
NM_001001548.3(CD36):c.-27C>T rs768286621 0.00013
NM_001001548.3(CD36):c.430-2A>G rs3211901 0.00013
NM_001001548.3(CD36):c.429+15A>G rs371196837 0.00012
NM_001001548.3(CD36):c.13C>T (p.Arg5Trp) rs752841786 0.00011
NM_001001547.3(CD36):c.-208C>T rs886062451 0.00010
NM_001001548.3(CD36):c.1279G>T (p.Ala427Ser) rs201527696 0.00009
NM_001001548.3(CD36):c.875G>T (p.Arg292Ile) rs200757788 0.00009
NM_001001547.3(CD36):c.-209C>T rs539733007 0.00007
NM_001001548.3(CD36):c.*1419+47A>G rs759397538 0.00006
NM_001001548.3(CD36):c.1254+5G>T rs371153088 0.00006
NM_001001548.3(CD36):c.282-14T>A rs754938089 0.00006
NM_001001548.3(CD36):c.318C>T (p.Asp106=) rs146796766 0.00006
NM_001001548.3(CD36):c.846C>T (p.Asp282=) rs749415195 0.00006
NM_001001548.3(CD36):c.1409C>T (p.Thr470Ile) rs200771788 0.00005
NM_001001548.3(CD36):c.-150T>A rs532897983 0.00004
NM_001001548.3(CD36):c.1254+1G>A rs148051111 0.00004
NM_001001548.3(CD36):c.625G>C (p.Asp209His) rs150674228 0.00004
NM_001001548.3(CD36):c.728G>A (p.Cys243Tyr) rs35793888 0.00004
NM_001001548.3(CD36):c.159T>C (p.Asn53=) rs886062452 0.00003
NM_001001548.3(CD36):c.410T>C (p.Val137Ala) rs2272350 0.00003
NM_001001548.3(CD36):c.429+5G>T rs753625642 0.00003
NM_001001548.3(CD36):c.44T>C (p.Ile15Thr) rs778587030 0.00003
NM_001001548.3(CD36):c.590C>T (p.Thr197Ile) rs757827176 0.00003
NM_001001548.3(CD36):c.609+1G>A rs755124649 0.00003
NM_001001548.3(CD36):c.682G>A (p.Asp228Asn) rs774794181 0.00003
NM_001001548.3(CD36):c.819-12C>A rs780361615 0.00003
NM_001001548.3(CD36):c.1045G>C (p.Ala349Pro) rs370701210 0.00002
NM_001001548.3(CD36):c.220C>T (p.Gln74Ter) rs545489204 0.00002
NM_001001548.3(CD36):c.491A>G (p.Lys164Arg) rs201801344 0.00002
NM_001001547.3(CD36):c.-206A>C rs1792285972 0.00001
NM_001001547.3(CD36):c.-286C>A rs886062450 0.00001
NM_001001547.3(CD36):c.-297G>A rs886062449 0.00001
NM_001001548.3(CD36):c.1126-15T>C rs758766716 0.00001
NM_001001548.3(CD36):c.281G>A (p.Arg94Lys) rs1796118367 0.00001
NM_001001548.3(CD36):c.355G>T (p.Gly119Cys) rs1250857302 0.00001
NM_001001548.3(CD36):c.456A>G (p.Gln152=) rs543785881 0.00001
NM_001001548.3(CD36):c.695G>T (p.Gly232Val) rs535150936 0.00001
NM_001001548.3(CD36):c.819-8G>A rs769908351 0.00001
NM_001001548.3(CD36):c.853C>T (p.Leu285=) rs780267115 0.00001
NM_001001547.3(CD36):c.-186T>G rs1455351951
NM_001001547.3(CD36):c.-325G>A rs886062448
NM_001001548.3(CD36):c.*1419+10T>C rs1798034310
NM_001001548.3(CD36):c.1112_1119dup (p.Glu374fs) rs1242969201
NM_001001548.3(CD36):c.1124C>T (p.Pro375Leu)
NM_001001548.3(CD36):c.1126-5_1127del rs770511058
NM_001001548.3(CD36):c.1181_1185dup (p.Glu397fs) rs757570230
NM_001001548.3(CD36):c.1200-12C>T rs765778656
NM_001001548.3(CD36):c.1220_1222del (p.Arg407del) rs773274847
NM_001001548.3(CD36):c.1254+1G>C
NM_001001548.3(CD36):c.1291A>G (p.Arg431Gly) rs140728267
NM_001001548.3(CD36):c.1297_1301del (p.Gln433fs) rs755620205
NM_001001548.3(CD36):c.1345_1348del (p.Leu449fs)
NM_001001548.3(CD36):c.14G>A (p.Arg5Gln) rs13306227
NM_001001548.3(CD36):c.265G>T (p.Gly89Cys) rs374729345
NM_001001548.3(CD36):c.275C>T (p.Thr92Met) rs150037612
NM_001001548.3(CD36):c.374C>T (p.Ser125Leu) rs886062453
NM_001001548.3(CD36):c.379_381dup (p.Ser127_Val128insSer)
NM_001001548.3(CD36):c.380C>G (p.Ser127Ter) rs201765331
NM_001001548.3(CD36):c.405C>G (p.Phe135Leu) rs747515126
NM_001001548.3(CD36):c.601T>C (p.Phe201Leu) rs1796699020
NM_001001548.3(CD36):c.610-5T>C rs185913608
NM_001001548.3(CD36):c.640G>A (p.Val214Ile) rs190735330
NM_001001548.3(CD36):c.689A>G (p.Tyr230Cys)
NM_001001548.3(CD36):c.701+1del rs775534351
NM_001001548.3(CD36):c.855del (p.Gly287fs)
NM_001001548.3(CD36):c.872A>G (p.Tyr291Cys) rs200752989
NM_001001548.3(CD36):c.907C>G (p.Pro303Ala) rs1797624389

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