ClinVar Miner

List of variants in gene SLX4 reported as benign for bone disorder

Included ClinVar conditions (1436):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 81
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HGVS dbSNP gnomAD frequency
NM_032444.4(SLX4):c.4500T>C (p.Asn1500=) rs3810812 0.63612
NM_032444.4(SLX4):c.753G>A (p.Ala251=) rs8061528 0.21914
NM_032444.4(SLX4):c.3365C>T (p.Pro1122Leu) rs714181 0.20077
NM_032444.4(SLX4):c.1366+11T>C rs76350200 0.08654
NM_032444.4(SLX4):c.2854G>A (p.Ala952Thr) rs59939128 0.07700
NM_032444.4(SLX4):c.2012T>C (p.Leu671Ser) rs77985244 0.07388
NM_032444.4(SLX4):c.610C>T (p.Arg204Cys) rs79842542 0.07023
NM_032444.4(SLX4):c.1371T>G (p.Asn457Lys) rs74319927 0.06397
NM_032444.4(SLX4):c.1156A>G (p.Met386Val) rs113490934 0.06384
NM_032444.4(SLX4):c.1152A>G (p.Pro384=) rs112511042 0.06311
NM_032444.4(SLX4):c.555C>T (p.Asp185=) rs74640850 0.04956
NM_032444.4(SLX4):c.2855C>T (p.Ala952Val) rs78637028 0.04953
NM_032444.4(SLX4):c.3662C>T (p.Ala1221Val) rs3827530 0.04930
NM_032444.4(SLX4):c.678C>T (p.His226=) rs28516461 0.04916
NM_032444.4(SLX4):c.3812C>T (p.Ser1271Phe) rs3810813 0.04718
NM_032444.4(SLX4):c.3162G>A (p.Ser1054=) rs76488917 0.03405
NM_032444.4(SLX4):c.4581G>A (p.Pro1527=) rs78635099 0.02283
NM_032444.4(SLX4):c.3783G>A (p.Pro1261=) rs77699867 0.02141
NM_032444.4(SLX4):c.2824G>C (p.Glu942Gln) rs114014006 0.01879
NM_032444.4(SLX4):c.3868C>A (p.His1290Asn) rs112596894 0.01345
NM_032444.4(SLX4):c.4338C>T (p.Thr1446=) rs77718962 0.00998
NM_032444.4(SLX4):c.5146T>A (p.Ser1716Thr) rs75182789 0.00995
NM_032444.4(SLX4):c.1153C>A (p.Pro385Thr) rs115694169 0.00924
NM_032444.4(SLX4):c.999C>T (p.Ile333=) rs7198338 0.00909
NM_032444.4(SLX4):c.2746G>T (p.Ala916Ser) rs79448721 0.00904
NM_032444.4(SLX4):c.4115G>A (p.Arg1372Gln) rs79174372 0.00861
NM_032444.4(SLX4):c.710G>A (p.Arg237Gln) rs138615800 0.00848
NM_032444.4(SLX4):c.1898G>A (p.Gly633Asp) rs1056085 0.00810
NM_032444.4(SLX4):c.5281C>T (p.Arg1761Cys) rs143818824 0.00776
NM_032444.4(SLX4):c.3963G>A (p.Pro1321=) rs116781836 0.00774
NM_032444.4(SLX4):c.1924+19C>A rs113075119 0.00694
NM_032444.4(SLX4):c.2924C>T (p.Pro975Leu) rs114472821 0.00668
NM_032444.4(SLX4):c.1803G>A (p.Ser601=) rs144892556 0.00649
NM_032444.4(SLX4):c.1755C>T (p.Pro585=) rs114016359 0.00638
NM_032444.4(SLX4):c.90C>T (p.Ser30=) rs118089506 0.00617
NM_032444.4(SLX4):c.5501A>G (p.Asn1834Ser) rs111738042 0.00575
NM_032444.4(SLX4):c.718A>G (p.Asn240Asp) rs114744903 0.00474
NM_032444.4(SLX4):c.1637A>G (p.Tyr546Cys) rs150547487 0.00416
NM_032444.4(SLX4):c.4600G>A (p.Gly1534Ser) rs78770603 0.00380
NM_032444.4(SLX4):c.4068G>A (p.Pro1356=) rs115491049 0.00367
NM_032444.4(SLX4):c.5029C>T (p.Pro1677Ser) rs7196345 0.00363
NM_032444.4(SLX4):c.336G>A (p.Pro112=) rs79126454 0.00362
NM_032444.4(SLX4):c.1802C>T (p.Ser601Leu) rs59706816 0.00333
NM_032444.4(SLX4):c.3857C>T (p.Ala1286Val) rs149011965 0.00296
NM_032444.4(SLX4):c.4241C>T (p.Pro1414Leu) rs140892471 0.00283
NM_032444.4(SLX4):c.4648C>T (p.Arg1550Trp) rs77021998 0.00210
NM_032444.4(SLX4):c.2328-9G>C rs73505419 0.00188
NM_032444.4(SLX4):c.3109T>C (p.Leu1037=) rs58735123 0.00148
NM_032444.4(SLX4):c.4024A>G (p.Ser1342Gly) rs140051968 0.00130
NM_032444.4(SLX4):c.2359G>A (p.Glu787Lys) rs140600202 0.00125
NM_032444.4(SLX4):c.590T>C (p.Val197Ala) rs147826749 0.00115
NM_032444.4(SLX4):c.3676C>T (p.Arg1226Trp) rs142008398 0.00114
NM_032444.4(SLX4):c.5259C>T (p.Asp1753=) rs144776083 0.00109
NM_032444.4(SLX4):c.4479G>A (p.Ser1493=) rs150097733 0.00100
NM_032444.4(SLX4):c.1372A>G (p.Lys458Glu) rs149126845 0.00087
NM_032444.4(SLX4):c.2786C>T (p.Pro929Leu) rs117707719 0.00078
NM_032444.4(SLX4):c.3178C>T (p.Arg1060Trp) rs144273492 0.00060
NM_032444.4(SLX4):c.2975G>A (p.Gly992Glu) rs139287784 0.00054
NM_032444.4(SLX4):c.2844G>A (p.Ala948=) rs376877866 0.00053
NM_032444.4(SLX4):c.4836C>T (p.Asp1612=) rs140844106 0.00051
NM_032444.4(SLX4):c.231A>G (p.Gln77=) rs143279888 0.00036
NM_032444.4(SLX4):c.86G>A (p.Arg29His) rs149117119 0.00026
NM_032444.4(SLX4):c.2628C>T (p.Asp876=) rs201279467 0.00016
NM_032444.4(SLX4):c.3315C>T (p.Ser1105=) rs183029626 0.00015
NM_032444.4(SLX4):c.2226C>T (p.Asp742=) rs376261173 0.00012
NM_032444.4(SLX4):c.2235C>T (p.Thr745=) rs75184268 0.00012
NM_032444.4(SLX4):c.1925-13A>T rs201324113 0.00011
NM_032444.4(SLX4):c.833G>A (p.Arg278Gln) rs201192909 0.00011
NM_032444.4(SLX4):c.630A>G (p.Leu210=) rs746155183 0.00008
NM_032444.4(SLX4):c.1511C>G (p.Pro504Arg) rs569591337 0.00007
NM_032444.4(SLX4):c.2034T>G (p.Val678=) rs200278096 0.00007
NM_032444.4(SLX4):c.3762G>A (p.Ser1254=) rs3810814 0.00007
NM_032444.4(SLX4):c.489T>G (p.Gly163=) rs201211891 0.00004
NM_032444.4(SLX4):c.5372G>A (p.Arg1791His) rs560381786 0.00004
NM_032444.4(SLX4):c.3245A>G (p.Gln1082Arg) rs368657696 0.00001
NM_032444.4(SLX4):c.1163+10C>G rs80116508
NM_032444.4(SLX4):c.1163+10C>T rs80116508
NM_032444.4(SLX4):c.1227G>A (p.Lys409=) rs534443134
NM_032444.4(SLX4):c.258AAG[1] (p.Arg87del) rs536289991
NM_032444.4(SLX4):c.2854_2855delinsAT (p.Ala952Met) rs863224277
NM_032444.4(SLX4):c.5154-4del rs2151116057

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