ClinVar Miner

List of variants in gene SLC26A5 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 51
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HGVS dbSNP gnomAD frequency
NM_198999.3(SLC26A5):c.1311+295G>A rs4285410 0.99907
NM_198999.3(SLC26A5):c.972-60A>G rs13240456 0.98475
NM_198999.3(SLC26A5):c.1677+77T>C rs12705120 0.98331
NM_198999.3(SLC26A5):c.1986+30T>C rs10273883 0.92836
NM_198999.3(SLC26A5):c.403+14T>C rs7779997 0.38939
NM_198999.3(SLC26A5):c.571-321A>G rs10275807 0.31388
NM_198999.3(SLC26A5):c.972-244C>T rs7804867 0.17521
NM_198999.3(SLC26A5):c.736-273G>C rs28446682 0.15062
NM_198999.3(SLC26A5):c.1312-44T>C rs62482415 0.13772
NM_206883.3(SLC26A5):c.2041+2675T>C rs28375913 0.11971
NM_198999.3(SLC26A5):c.2041+232G>A rs62482412 0.08071
NM_198999.3(SLC26A5):c.1233+292A>G rs72655388 0.07220
NM_198999.3(SLC26A5):c.1234-218A>G rs79723233 0.07146
NM_198999.3(SLC26A5):c.1312-49C>T rs56373660 0.06714
NM_198999.3(SLC26A5):c.1120-257G>A rs55801500 0.03206
NM_198999.3(SLC26A5):c.889-85C>G rs75861002 0.02562
NM_198999.3(SLC26A5):c.1233+143G>A rs74584081 0.02492
NM_198999.3(SLC26A5):c.1311+212G>C rs4604353 0.02489
NM_198999.3(SLC26A5):c.1515-44C>T rs72655395 0.02481
NM_198999.3(SLC26A5):c.570+6G>A rs113889101 0.02425
NM_198999.3(SLC26A5):c.571-283A>G rs113982096 0.02306
NM_198999.3(SLC26A5):c.2041+107T>C rs72655393 0.02067
NM_198999.3(SLC26A5):c.1514+187A>G rs79997385 0.01736
NM_198999.3(SLC26A5):c.735+303A>G rs116674459 0.01716
NM_198999.3(SLC26A5):c.293-318G>A rs116627976 0.01620
NM_198999.3(SLC26A5):c.1312-76G>A rs72655391 0.01602
NM_198999.3(SLC26A5):c.989A>G (p.Asn330Ser) rs117444825 0.00944
NM_198999.3(SLC26A5):c.-53-2A>G rs116900495 0.00746
NM_198999.3(SLC26A5):c.1335T>C (p.Ile445=) rs142639517 0.00364
NM_198999.3(SLC26A5):c.137T>C (p.Leu46Pro) rs141952919 0.00266
NM_198999.3(SLC26A5):c.-13A>C rs142432368 0.00252
NM_198999.3(SLC26A5):c.1813A>G (p.Thr605Ala) rs142849754 0.00206
NM_198999.3(SLC26A5):c.153-10G>A rs200680274 0.00143
NM_198999.3(SLC26A5):c.1590A>G (p.Lys530=) rs138432667 0.00135
NM_198999.3(SLC26A5):c.1302A>G (p.Ser434=) rs72655380 0.00068
NM_198999.3(SLC26A5):c.1572C>T (p.Asp524=) rs191358470 0.00044
NM_198999.3(SLC26A5):c.2042-5A>G rs188738404 0.00038
NM_198999.3(SLC26A5):c.2184T>G (p.Pro728=) rs534530722 0.00001
NM_198999.3(SLC26A5):c.1585-163dup rs375313152
NM_198999.3(SLC26A5):c.1678-323G>C rs62482413
NM_198999.3(SLC26A5):c.2041+120_2041+122del rs66928926
NM_198999.3(SLC26A5):c.2042-85del rs556110302
NM_198999.3(SLC26A5):c.2042-95dup rs556110302
NM_198999.3(SLC26A5):c.403+151C>T rs7780218
NM_198999.3(SLC26A5):c.570+86C>T rs56305143
NM_198999.3(SLC26A5):c.888+217_888+218del rs111663534
NM_198999.3(SLC26A5):c.971+179_971+180del rs141013688
NM_198999.3(SLC26A5):c.971+200_971+202dup rs72106385
NM_198999.3(SLC26A5):c.971+200dup rs72106385
NM_198999.3(SLC26A5):c.971+215del rs72106385
NM_206883.2(SLC26A5):c.292+8_292+9dup rs112791865

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