ClinVar Miner

List of variants reported as uncertain risk allele for Wolfram syndrome

Included ClinVar conditions (10):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 63
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HGVS dbSNP gnomAD frequency
NM_006005.3(WFS1):c.1726G>A (p.Gly576Ser) rs1805069 0.01068
NM_006005.3(WFS1):c.2335G>A (p.Val779Met) rs141328044 0.00672
NM_006005.3(WFS1):c.2039A>C (p.Glu680Ala) rs144840779 0.00050
NM_006005.3(WFS1):c.1706C>T (p.Ala569Val) rs144492050 0.00042
NM_006005.3(WFS1):c.1693C>G (p.Leu565Val) rs200058166 0.00030
NM_006005.3(WFS1):c.1024G>A (p.Ala342Thr) rs148028521 0.00029
NM_006005.3(WFS1):c.1817T>G (p.Val606Gly) rs756252214 0.00011
NM_006005.3(WFS1):c.1969A>G (p.Met657Val) rs71532861 0.00010
NM_006005.3(WFS1):c.695G>A (p.Arg232His) rs375904080 0.00010
NM_006005.3(WFS1):c.976G>A (p.Ala326Thr) rs200790641 0.00009
NM_006005.3(WFS1):c.2119G>A (p.Val707Ile) rs71524377 0.00007
NM_006005.3(WFS1):c.1580C>T (p.Thr527Ile) rs372663248 0.00006
NM_006005.3(WFS1):c.1886G>A (p.Arg629Gln) rs146670741 0.00006
NM_006005.3(WFS1):c.2029G>A (p.Ala677Thr) rs757027394 0.00005
NM_006005.3(WFS1):c.2414G>A (p.Arg805Gln) rs140667597 0.00005
NM_006005.3(WFS1):c.2299A>C (p.Ile767Leu) rs779199009 0.00004
NM_006005.3(WFS1):c.2225G>A (p.Cys742Tyr) rs775216682 0.00003
NM_006005.3(WFS1):c.2632G>A (p.Ala878Thr) rs570527044 0.00003
NM_006005.3(WFS1):c.95C>T (p.Ser32Leu) rs727504730 0.00003
NM_006005.3(WFS1):c.991T>A (p.Phe331Ile) rs144888979 0.00003
NM_006005.3(WFS1):c.2560C>T (p.Leu854Phe) rs771391168 0.00002
NM_006005.3(WFS1):c.727G>A (p.Ala243Thr) rs760226129 0.00002
NM_006005.3(WFS1):c.1103G>A (p.Ser368Asn) rs397517194 0.00001
NM_006005.3(WFS1):c.1106A>C (p.Lys369Thr) rs766169444 0.00001
NM_006005.3(WFS1):c.1122C>G (p.Phe374Leu) rs1235126935 0.00001
NM_006005.3(WFS1):c.115G>A (p.Glu39Lys) rs774330485 0.00001
NM_006005.3(WFS1):c.1676C>T (p.Ala559Val) rs773343292 0.00001
NM_006005.3(WFS1):c.1837T>G (p.Trp613Gly) rs1730924133 0.00001
NM_006005.3(WFS1):c.2074C>T (p.His692Tyr) rs1131691259 0.00001
NM_006005.3(WFS1):c.2182G>A (p.Gly728Ser) rs202195756 0.00001
NM_006005.3(WFS1):c.2192T>C (p.Met731Thr) rs146418094 0.00001
NM_006005.3(WFS1):c.2285A>G (p.Lys762Arg) rs876658119 0.00001
NM_006005.3(WFS1):c.382G>T (p.Asp128Tyr) rs71524350 0.00001
NM_006005.3(WFS1):c.535G>A (p.Ala179Thr) rs776685250 0.00001
NM_006005.3(WFS1):c.578A>G (p.Lys193Arg) rs1005714777 0.00001
NM_006005.3(WFS1):c.601C>A (p.Leu201Met) rs529580583 0.00001
NM_006005.3(WFS1):c.634G>A (p.Gly212Arg) rs1216952842 0.00001
NM_006005.3(WFS1):c.70C>T (p.Arg24Cys) rs756667462 0.00001
NM_006005.3(WFS1):c.716A>G (p.Lys239Arg) rs727503747 0.00001
NM_006005.3(WFS1):c.83A>G (p.Asn28Ser) rs397517198 0.00001
NM_006005.3(WFS1):c.968A>T (p.His323Leu) rs1057368575 0.00001
NM_006005.3(WFS1):c.994A>T (p.Ile332Phe) rs564413149 0.00001
NM_006005.3(WFS1):c.1142T>C (p.Leu381Pro) rs797046111
NM_006005.3(WFS1):c.1162C>G (p.Leu388Val) rs1578609065
NM_006005.3(WFS1):c.1192G>A (p.Gly398Ser) rs863224269
NM_006005.3(WFS1):c.1210C>G (p.Pro404Ala) rs756869880
NM_006005.3(WFS1):c.1572C>G (p.Phe524Leu) rs1553878608
NM_006005.3(WFS1):c.1739T>A (p.Val580Glu) rs140773453
NM_006005.3(WFS1):c.1836G>C (p.Trp612Cys) rs775158434
NM_006005.3(WFS1):c.1868T>A (p.Met623Lys) rs758746685
NM_006005.3(WFS1):c.2030C>G (p.Ala677Gly) rs1730936563
NM_006005.3(WFS1):c.2032T>G (p.Trp678Gly) rs1578611784
NM_006005.3(WFS1):c.2041A>G (p.Thr681Ala) rs1353393888
NM_006005.3(WFS1):c.2082G>C (p.Glu694Asp) rs751270928
NM_006005.3(WFS1):c.2183G>A (p.Gly728Asp) rs1560421124
NM_006005.3(WFS1):c.2278C>A (p.Leu760Met) rs1553878931
NM_006005.3(WFS1):c.2296C>T (p.His766Tyr) rs1553878946
NM_006005.3(WFS1):c.2298C>A (p.His766Gln) rs755328574
NM_006005.3(WFS1):c.2389G>A (p.Asp797Asn) rs1553879004
NM_006005.3(WFS1):c.2480C>T (p.Thr827Ile) rs1730968164
NM_006005.3(WFS1):c.881A>T (p.His294Leu) rs727503748
NM_006005.3(WFS1):c.955A>T (p.Ile319Phe) rs914996283
NM_006005.3(WFS1):c.958C>T (p.Pro320Ser) rs1553878280

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