ClinVar Miner

List of variants in gene DYSF reported as benign by GeneDx

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 138
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HGVS dbSNP
NC_000002.12:g.71453502T>C
NC_000002.12:g.71482001C>G
NC_000002.12:g.71528250A>G
NC_000002.12:g.71552987C>G
NC_000002.12:g.71611370del
NC_000002.12:g.71644106A>G
NC_000002.12:g.71664231C>T
NC_000002.12:g.71674156C>T
NM_001130987.2(DYSF):c.-128G>A
NM_001130987.2(DYSF):c.-30G>A
NM_001130987.2(DYSF):c.1002+216C>T
NM_001130987.2(DYSF):c.1003-73A>G
NM_001130987.2(DYSF):c.1033+230G>T
NM_001130987.2(DYSF):c.1033+94G>T
NM_001130987.2(DYSF):c.1034-196C>G
NM_001130987.2(DYSF):c.1034-20G>A rs12713756
NM_001130987.2(DYSF):c.1034-64C>T
NM_001130987.2(DYSF):c.1034-68T>C
NM_001130987.2(DYSF):c.1038C>T (p.His346=) rs36122356
NM_001130987.2(DYSF):c.1134T>C (p.Pro378=) rs571559303
NM_001130987.2(DYSF):c.1149+54C>T
NM_001130987.2(DYSF):c.1216G>C (p.Val406Leu) rs150724610
NM_001130987.2(DYSF):c.1276+11C>T rs35982795
NM_001130987.2(DYSF):c.1380+136C>T
NM_001130987.2(DYSF):c.1380+6G>C rs75796187
NM_001130987.2(DYSF):c.1449+13C>T rs4852801
NM_001130987.2(DYSF):c.1450-88A>G
NM_001130987.2(DYSF):c.148-277T>C
NM_001130987.2(DYSF):c.1494-163G>T
NM_001130987.2(DYSF):c.1518C>T (p.Ile506=) rs34387018
NM_001130987.2(DYSF):c.1576+118G>A
NM_001130987.2(DYSF):c.1576+253T>A
NM_001130987.2(DYSF):c.1577-103G>A
NM_001130987.2(DYSF):c.1577-1635C>G rs76402294
NM_001130987.2(DYSF):c.1577-1825A>G
NM_001130987.2(DYSF):c.1577-1826C>T
NM_001130987.2(DYSF):c.1693-62C>T
NM_001130987.2(DYSF):c.1785G>A (p.Ala595=) rs35984374
NM_001130987.2(DYSF):c.1806+182G>A
NM_001130987.2(DYSF):c.1806+265C>T
NM_001130987.2(DYSF):c.1807-288T>C
NM_001130987.2(DYSF):c.1881T>C (p.Asp627=) rs2303596
NM_001130987.2(DYSF):c.1914C>T (p.Tyr638=) rs35721373
NM_001130987.2(DYSF):c.1944G>A (p.Pro648=) rs115849497
NM_001130987.2(DYSF):c.1985-116T>C
NM_001130987.2(DYSF):c.2110-331C>G
NM_001130987.2(DYSF):c.2216+16C>T rs111389127
NM_001130987.2(DYSF):c.239+20G>A rs12470028
NM_001130987.2(DYSF):c.240-289G>A
NM_001130987.2(DYSF):c.2554A>G (p.Ile852Val) rs34671418
NM_001130987.2(DYSF):c.2565+234G>T
NM_001130987.2(DYSF):c.2637A>T (p.Ser879=) rs2288355
NM_001130987.2(DYSF):c.2642A>C (p.Asp881Ala) rs35884879
NM_001130987.2(DYSF):c.2856G>A (p.Pro952=) rs34836829
NM_001130987.2(DYSF):c.2864+244G>C
NM_001130987.2(DYSF):c.2864+84G>C
NM_001130987.2(DYSF):c.2865-85C>G
NM_001130987.2(DYSF):c.2979+112A>C
NM_001130987.2(DYSF):c.3086-17G>A rs3764971
NM_001130987.2(DYSF):c.3119G>A (p.Arg1040Gln) rs34211915
NM_001130987.2(DYSF):c.3229-306G>A
NM_001130987.2(DYSF):c.3229-61G>C
NM_001130987.2(DYSF):c.3239_3244CGGAGG[3] (p.1080_1081AE[3]) rs398123779
NM_001130987.2(DYSF):c.3337C>T (p.Arg1113Cys) rs141536854
NM_001130987.2(DYSF):c.3341G>A (p.Arg1114His) rs59915619
NM_001130987.2(DYSF):c.3403-112T>C
NM_001130987.2(DYSF):c.3403-121G>C
NM_001130987.2(DYSF):c.3496+187A>G
NM_001130987.2(DYSF):c.3575-17C>T rs13421969
NM_001130987.2(DYSF):c.3575-256G>C
NM_001130987.2(DYSF):c.3588C>T (p.Ile1196=) rs79899601
NM_001130987.2(DYSF):c.3756+133T>C
NM_001130987.2(DYSF):c.3756+134A>T
NM_001130987.2(DYSF):c.3756+202T>C
NM_001130987.2(DYSF):c.3756+227C>T
NM_001130987.2(DYSF):c.3757-12C>T rs114968209
NM_001130987.2(DYSF):c.3757-277C>T
NM_001130987.2(DYSF):c.386G>A (p.Gly129Glu) rs34997054
NM_001130987.2(DYSF):c.3898-206A>T
NM_001130987.2(DYSF):c.3928-85G>T
NM_001130987.2(DYSF):c.3958-79C>T
NM_001130987.2(DYSF):c.396C>T (p.Pro132=) rs34603128
NM_001130987.2(DYSF):c.4026C>T (p.Asn1342=) rs11558179
NM_001130987.2(DYSF):c.4046G>T (p.Arg1349Leu) rs61742872
NM_001130987.2(DYSF):c.4062C>A (p.Ile1354=) rs2303606
NM_001130987.2(DYSF):c.4122C>T (p.Ser1374=) rs2303607
NM_001130987.2(DYSF):c.4221+119A>G
NM_001130987.2(DYSF):c.4221+96C>T
NM_001130987.2(DYSF):c.4222-20G>A rs111935215
NM_001130987.2(DYSF):c.4377G>A (p.Gln1459=) rs76576806
NM_001130987.2(DYSF):c.4388-246C>T
NM_001130987.2(DYSF):c.4430A>G (p.Asp1477Gly) rs61738567
NM_001130987.2(DYSF):c.4527+204C>A
NM_001130987.2(DYSF):c.4528-127C>T
NM_001130987.2(DYSF):c.4528-56A>G
NM_001130987.2(DYSF):c.460+150A>G
NM_001130987.2(DYSF):c.460+17G>C rs115170960
NM_001130987.2(DYSF):c.460+222G>A
NM_001130987.2(DYSF):c.460+243G>A
NM_001130987.2(DYSF):c.4621C>T (p.Leu1541=) rs7573406
NM_001130987.2(DYSF):c.4627-305C>T
NM_001130987.2(DYSF):c.4848G>A (p.Glu1616=) rs62145939
NM_001130987.2(DYSF):c.4937T>C (p.Ile1646Thr) rs146384562
NM_001130987.2(DYSF):c.5003+1320A>G
NM_001130987.2(DYSF):c.5003+1375C>G
NM_001130987.2(DYSF):c.5003+1380G>A
NM_001130987.2(DYSF):c.5003+1393G>A
NM_001130987.2(DYSF):c.5004-162C>T
NM_001130987.2(DYSF):c.5318-225A>G
NM_001130987.2(DYSF):c.5784+199A>G
NM_001130987.2(DYSF):c.5785-185G>A
NM_001130987.2(DYSF):c.5885-16T>C rs1863812
NM_001130987.2(DYSF):c.5976A>C (p.Pro1992=) rs17718530
NM_001130987.2(DYSF):c.605C>A (p.Ala202Glu) rs34999029
NM_001130987.2(DYSF):c.6064-201G>T
NM_001130987.2(DYSF):c.6064-273A>G
NM_001130987.2(DYSF):c.6174-297T>C
NM_001130987.2(DYSF):c.6321+15C>T rs2559082
NM_001130987.2(DYSF):c.661C>G (p.Leu221Val) rs13407355
NM_001130987.2(DYSF):c.666T>C (p.Pro222=) rs35392229
NM_001130987.2(DYSF):c.759+206G>C
NM_001130987.2(DYSF):c.760-17C>T rs61104194
NM_001130987.2(DYSF):c.777C>T (p.Ile259=) rs138054675
NM_001130987.2(DYSF):c.888+11T>C rs13428076
NM_001130987.2(DYSF):c.888+97T>C
NM_001130987.2(DYSF):c.889-104G>A
NM_001130987.2(DYSF):c.889-68G>A
NM_001130987.2(DYSF):c.91+280A>G
NM_001130987.2(DYSF):c.951+268T>C
NM_001130987.2(DYSF):c.951+4T>C rs11903960
NM_001130987.2(DYSF):c.951+82A>G
NM_001130987.2(DYSF):c.951+83C>T
NM_001130987.2(DYSF):c.952-135C>T
NM_003494.4(DYSF):c.-179C>A
NM_003494.4(DYSF):c.-34G>T rs192358316
NM_003494.4(DYSF):c.88+12437C>T
NM_003494.4(DYSF):c.88+12487C>A
NM_003494.4(DYSF):c.88+12589T>C

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