ClinVar Miner

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

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Gene type:
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Total variants: 100
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HGVS dbSNP
NC_000002.12:g.71453502T>C
NC_000002.12:g.71611370del
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.1034-64C>T
NM_001130987.2(DYSF):c.1034-68T>C
NM_001130987.2(DYSF):c.1038C>T (p.His346=) rs36122356
NM_001130987.2(DYSF):c.1149+54C>T
NM_001130987.2(DYSF):c.1216G>C (p.Val406Leu) rs150724610
NM_001130987.2(DYSF):c.1277-48A>G rs4852800
NM_001130987.2(DYSF):c.1380+136C>T
NM_001130987.2(DYSF):c.1450-88A>G
NM_001130987.2(DYSF):c.1465G>A (p.Glu489Lys) rs61740288
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.1577-1825A>G
NM_001130987.2(DYSF):c.1577-1826C>T
NM_001130987.2(DYSF):c.1693-62C>T
NM_001130987.2(DYSF):c.1806+182G>A
NM_001130987.2(DYSF):c.1806+265C>T
NM_001130987.2(DYSF):c.1807-24C>G rs2303595
NM_001130987.2(DYSF):c.1807-288T>C
NM_001130987.2(DYSF):c.1881T>C (p.Asp627=) rs2303596
NM_001130987.2(DYSF):c.1985-116T>C
NM_001130987.2(DYSF):c.2110-331C>G
NM_001130987.2(DYSF):c.225G>A (p.Thr75=) rs200957354
NM_001130987.2(DYSF):c.239+31C>G rs78958249
NM_001130987.2(DYSF):c.240-289G>A
NM_001130987.2(DYSF):c.2565+234G>T
NM_001130987.2(DYSF):c.2637A>T (p.Ser879=) rs2288355
NM_001130987.2(DYSF):c.2817G>A (p.Ser939=) rs148902254
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.3229-306G>A
NM_001130987.2(DYSF):c.3229-61G>C
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.3575-256G>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.3757-277C>T
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.4062C>A (p.Ile1354=) rs2303606
NM_001130987.2(DYSF):c.4221+119A>G
NM_001130987.2(DYSF):c.4221+96C>T
NM_001130987.2(DYSF):c.4377G>A (p.Gln1459=) rs76576806
NM_001130987.2(DYSF):c.4388-246C>T
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+222G>A
NM_001130987.2(DYSF):c.460+243G>A
NM_001130987.2(DYSF):c.4626+43A>G rs84182
NM_001130987.2(DYSF):c.4627-305C>T
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.5004-37C>T rs2303599
NM_001130987.2(DYSF):c.5058C>A (p.Leu1686=) rs141476432
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.5785-41C>T rs2559081
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.759+206G>C
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+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.88+12437C>T
NM_003494.4(DYSF):c.88+12487C>A
NM_003494.4(DYSF):c.88+12589T>C

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