ClinVar Miner

List of variants in gene SLC6A19 reported as benign for not provided

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Gene type:
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Total variants: 56
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HGVS dbSNP gnomAD frequency
NM_001003841.3(SLC6A19):c.1539-67T>C rs12513763 0.93561
NM_001003841.3(SLC6A19):c.1378+94C>T rs6554668 0.91904
NM_001003841.3(SLC6A19):c.990A>G (p.Thr330=) rs4975629 0.91839
NM_001003841.3(SLC6A19):c.1538+95G>A rs6869718 0.90064
NC_000005.10:g.1201349A>G rs7379677 0.82628
NM_001003841.3(SLC6A19):c.306T>C (p.Gly102=) rs60992377 0.39132
NM_001003841.3(SLC6A19):c.663+48C>T rs13180809 0.38844
NM_001003841.3(SLC6A19):c.343+62A>T rs72709422 0.38153
NM_001003841.3(SLC6A19):c.1538+80C>T rs11746371 0.36715
NM_001003841.3(SLC6A19):c.664-68C>T rs77928413 0.35663
NM_001003841.3(SLC6A19):c.1174-90C>T rs6865308 0.35198
NM_001003841.3(SLC6A19):c.1017-4G>A rs35329108 0.25295
NM_001003841.3(SLC6A19):c.481+93G>A rs4358564 0.22183
NM_001003841.3(SLC6A19):c.754G>A (p.Val252Ile) rs7732589 0.18781
NM_001003841.3(SLC6A19):c.202+175C>T rs13188961 0.18573
NC_000005.10:g.1201391C>T rs7381010 0.17996
NM_001003841.3(SLC6A19):c.343+192C>G rs74938348 0.11264
NM_001003841.3(SLC6A19):c.343+184C>G rs76678756 0.11262
NM_001003841.3(SLC6A19):c.-8C>T rs67330201 0.06178
NM_001003841.3(SLC6A19):c.663+16G>A rs75252137 0.06012
NM_001003841.3(SLC6A19):c.1173+14G>A rs76207842 0.05574
NM_001003841.3(SLC6A19):c.202+33C>T rs13188787 0.03531
NM_001003841.3(SLC6A19):c.*148C>T rs113452990 0.03248
NM_001003841.3(SLC6A19):c.1174-156C>A rs113860722 0.02815
NM_001003841.3(SLC6A19):c.888-3C>T rs114350709 0.02512
NM_001003841.3(SLC6A19):c.*152T>C rs193050049 0.02377
NM_001003841.3(SLC6A19):c.1002C>T (p.Asp334=) rs60893203 0.02121
NM_001003841.3(SLC6A19):c.1173+52C>T rs116283705 0.01700
NM_001003841.3(SLC6A19):c.1701C>T (p.Tyr567=) rs139211708 0.01392
NM_001003841.3(SLC6A19):c.966C>T (p.Tyr322=) rs115133359 0.01389
NM_001003841.3(SLC6A19):c.664-51A>G rs111815477 0.01302
NM_001003841.3(SLC6A19):c.343+15G>A rs6865548 0.00987
NM_001003841.3(SLC6A19):c.327G>A (p.Pro109=) rs114684753 0.00447
NM_001003841.3(SLC6A19):c.984C>T (p.Arg328=) rs140296083 0.00292
NM_001003841.3(SLC6A19):c.555G>A (p.Thr185=) rs115871703 0.00268
NM_001003841.3(SLC6A19):c.775-5C>T rs149379208 0.00222
NM_001003841.3(SLC6A19):c.117G>A (p.Ala39=) rs149830504 0.00197
NM_001003841.3(SLC6A19):c.775-4G>A rs144753758 0.00158
NM_001003841.3(SLC6A19):c.114G>A (p.Lys38=) rs139908611 0.00153
NM_001003841.3(SLC6A19):c.156C>T (p.Leu52=) rs146382764 0.00139
NM_001003841.3(SLC6A19):c.41G>A (p.Arg14Gln) rs147458082 0.00128
NM_001003841.3(SLC6A19):c.276C>T (p.Ile92=) rs146678323 0.00078
NM_001003841.3(SLC6A19):c.558C>T (p.Ser186=) rs140343487 0.00073
NM_001003841.3(SLC6A19):c.813G>A (p.Ala271=) rs113308807 0.00073
NM_001003841.3(SLC6A19):c.343+11C>T rs146085736 0.00053
NM_001003841.3(SLC6A19):c.45C>G (p.Ile15Met) rs138390777 0.00052
NM_001003841.3(SLC6A19):c.48G>A (p.Pro16=) rs141911612 0.00034
NM_001003841.3(SLC6A19):c.849C>T (p.Phe283=) rs201416473 0.00011
NM_001003841.3(SLC6A19):c.482-12C>T rs199580276 0.00009
NM_001003841.3(SLC6A19):c.1173+163G>C rs6554665
NM_001003841.3(SLC6A19):c.1379-9G>C rs80151745
NM_001003841.3(SLC6A19):c.343+37_343+75del rs774243050
NM_001003841.3(SLC6A19):c.482-61C>A rs7727745
NM_001003841.3(SLC6A19):c.554C>T (p.Thr185Met)
NM_001003841.3(SLC6A19):c.775-60_775-58del rs138649942
NM_001003841.3(SLC6A19):c.887+84A>G rs6554663

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