ClinVar Miner

List of variants in gene WFS1 reported as benign for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 62
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HGVS dbSNP
NM_006005.3(WFS1):c.*131C>T rs55993016
NM_006005.3(WFS1):c.*149G>A rs1046320
NM_006005.3(WFS1):c.*241T>C rs60985011
NM_006005.3(WFS1):c.*242G>C rs80055761
NM_006005.3(WFS1):c.*253G>A rs1046322
NM_006005.3(WFS1):c.*274A>G rs1046325
NM_006005.3(WFS1):c.*333C>A rs111800114
NM_006005.3(WFS1):c.*358T>C
NM_006005.3(WFS1):c.*47T>C rs1046317
NM_006005.3(WFS1):c.*512C>T rs71528900
NM_006005.3(WFS1):c.*54A>G rs71526455
NM_006005.3(WFS1):c.*567C>G rs12508118
NM_006005.3(WFS1):c.*604G>C rs9457
NM_006005.3(WFS1):c.*637T>C rs71528901
NM_006005.3(WFS1):c.*683C>T rs3200
NM_006005.3(WFS1):c.*69C>T
NM_006005.3(WFS1):c.*90G>A rs1802453
NM_006005.3(WFS1):c.*91C>T rs1046319
NM_006005.3(WFS1):c.-6+11C>T rs547998667
NM_006005.3(WFS1):c.1023C>T (p.Phe341=) rs56072215
NM_006005.3(WFS1):c.1134C>A (p.Thr378=) rs71530904
NM_006005.3(WFS1):c.1185C>T (p.Val395=) rs1801206
NM_006005.3(WFS1):c.1294C>G (p.Leu432Val) rs35031397
NM_006005.3(WFS1):c.1308C>T (p.Thr436=) rs71539646
NM_006005.3(WFS1):c.1500C>T (p.Asn500=) rs1801214
NM_006005.3(WFS1):c.1674C>T (p.Arg558=) rs61735402
NM_006005.3(WFS1):c.1683C>T (p.Ile561=) rs71530906
NM_006005.3(WFS1):c.1725C>T (p.Ala575=) rs2230719
NM_006005.3(WFS1):c.1797C>A (p.Val599=) rs71524361
NM_006005.3(WFS1):c.1800C>T (p.Thr600=) rs71524362
NM_006005.3(WFS1):c.1832G>A (p.Arg611His) rs734312
NM_006005.3(WFS1):c.2019C>T (p.Cys673=) rs71524375
NM_006005.3(WFS1):c.2040G>A (p.Glu680=) rs375263408
NM_006005.3(WFS1):c.2124C>T (p.Arg708=) rs61735401
NM_006005.3(WFS1):c.2184C>T (p.Gly728=) rs71530908
NM_006005.3(WFS1):c.21G>T (p.Pro7=) rs372928810
NM_006005.3(WFS1):c.2205C>T (p.Tyr735=) rs71530911
NM_006005.3(WFS1):c.2209G>A (p.Glu737Lys) rs147834269
NM_006005.3(WFS1):c.2247G>A (p.Thr749=) rs75096624
NM_006005.3(WFS1):c.225C>T (p.Asp75=) rs35216268
NM_006005.3(WFS1):c.2322G>A (p.Lys774=) rs2230721
NM_006005.3(WFS1):c.2327A>T (p.Glu776Val) rs56002719
NM_006005.3(WFS1):c.2370G>A (p.Ser790=) rs150936382
NM_006005.3(WFS1):c.2433G>A (p.Lys811=) rs1046314
NM_006005.3(WFS1):c.2452C>T (p.Arg818Cys) rs35932623
NM_006005.3(WFS1):c.2565A>G (p.Ser855=) rs1046316
NM_006005.3(WFS1):c.2611G>A (p.Val871Met) rs71532874
NM_006005.3(WFS1):c.315+11C>T rs202232817
NM_006005.3(WFS1):c.402G>A (p.Ala134=) rs199533137
NM_006005.3(WFS1):c.461-15C>T rs9998519
NM_006005.3(WFS1):c.461-9A>G rs10010131
NM_006005.3(WFS1):c.482G>A (p.Arg161Gln) rs115346085
NM_006005.3(WFS1):c.510C>G (p.Thr170=) rs151277039
NM_006005.3(WFS1):c.577A>C (p.Lys193Gln) rs41264699
NM_006005.3(WFS1):c.684C>G (p.Arg228=) rs1801213
NM_006005.3(WFS1):c.712+16G>A rs71524367
NM_006005.3(WFS1):c.713-1075C>G rs6446482
NM_006005.3(WFS1):c.854G>A (p.Arg285His) rs61735404
NM_006005.3(WFS1):c.917T>C (p.Met306Thr) rs146114074
NM_006005.3(WFS1):c.930A>G (p.Ala310=) rs115561278
NM_006005.3(WFS1):c.997G>A (p.Val333Ile) rs1801212
NM_006005.3(WFS1):c.9C>T (p.Ser3=) rs71524363

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