NM_001374353.1(GLI2):c.3865G>A (p.Asp1289Asn)
|
rs12711538
|
0.66550
|
NM_001374353.1(GLI2):c.3888A>G (p.Pro1296=)
|
rs10167980
|
0.61468
|
NM_001374353.1(GLI2):c.3415G>T (p.Ala1139Ser)
|
rs3738880
|
0.61025
|
NM_001374353.1(GLI2):c.2889C>T (p.Ser963=)
|
rs146811565
|
0.04735
|
NM_001374353.1(GLI2):c.2997C>T (p.Asp999=)
|
rs140479803
|
0.02616
|
NM_001374353.1(GLI2):c.3892C>T (p.Pro1298Ser)
|
rs114376238
|
0.01651
|
NM_001374353.1(GLI2):c.4003A>G (p.Met1335Val)
|
rs149140724
|
0.00970
|
NM_001374353.1(GLI2):c.4507G>A (p.Asp1503Asn)
|
rs114814747
|
0.00964
|
NM_001374353.1(GLI2):c.3539G>A (p.Gly1180Asp)
|
rs114823319
|
0.00522
|
NM_001374353.1(GLI2):c.720C>T (p.Asp240=)
|
rs142793481
|
0.00483
|
NM_001374353.1(GLI2):c.4281G>A (p.Met1427Ile)
|
rs146467786
|
0.00465
|
NM_001374353.1(GLI2):c.4282C>T (p.Leu1428Phe)
|
rs146207623
|
0.00465
|
NM_001374353.1(GLI2):c.4612T>C (p.Ser1538Pro)
|
rs144372453
|
0.00352
|
NM_001374353.1(GLI2):c.2037A>G (p.Ala679=)
|
rs146059306
|
0.00325
|
NM_001374353.1(GLI2):c.2967C>T (p.Gly989=)
|
rs373880077
|
0.00285
|
NM_001374353.1(GLI2):c.3298G>T (p.Val1100Leu)
|
rs147580961
|
0.00222
|
NM_001374353.1(GLI2):c.3477G>T (p.Gln1159His)
|
rs139686081
|
0.00181
|
NM_001374353.1(GLI2):c.1935G>A (p.Ser645=)
|
rs114259687
|
0.00177
|
NM_001374353.1(GLI2):c.1243G>A (p.Val415Met)
|
rs142296407
|
0.00124
|
NM_001374353.1(GLI2):c.1808C>T (p.Thr603Met)
|
rs142775128
|
0.00099
|
NM_001374353.1(GLI2):c.2939C>G (p.Pro980Arg)
|
rs563818052
|
0.00088
|
NM_001374353.1(GLI2):c.607G>A (p.Ala203Thr)
|
rs147044066
|
0.00088
|
NM_001374353.1(GLI2):c.1080G>A (p.Ser360=)
|
rs149110951
|
0.00073
|
NM_001374353.1(GLI2):c.3979C>T (p.Leu1327=)
|
rs149290823
|
0.00073
|
NM_001374353.1(GLI2):c.4577G>A (p.Arg1526His)
|
rs138987487
|
0.00059
|
NM_001374353.1(GLI2):c.2034G>A (p.Thr678=)
|
rs139298853
|
0.00041
|
NM_001374353.1(GLI2):c.3309C>T (p.Ser1103=)
|
rs145751002
|
0.00035
|
NM_001374353.1(GLI2):c.2251C>T (p.Leu751=)
|
rs200831069
|
0.00033
|
NM_001374353.1(GLI2):c.4506C>T (p.Gly1502=)
|
rs200499325
|
0.00020
|
NM_001374353.1(GLI2):c.132G>A (p.Ala44=)
|
rs145778937
|
0.00017
|
NM_001374353.1(GLI2):c.221A>G (p.His74Arg)
|
rs377700501
|
0.00016
|
NM_001374353.1(GLI2):c.4147G>T (p.Gly1383Cys)
|
rs143914758
|
0.00013
|
NM_001374353.1(GLI2):c.2886G>A (p.Leu962=)
|
rs777165274
|
0.00012
|
NM_001374353.1(GLI2):c.1875C>T (p.His625=)
|
rs372341303
|
0.00007
|
NM_001374353.1(GLI2):c.1120C>T (p.Arg374Cys)
|
rs200076785
|
0.00006
|
NM_001374353.1(GLI2):c.315G>A (p.Pro105=)
|
rs139473153
|
0.00006
|
NM_001374353.1(GLI2):c.1701T>C (p.His567=)
|
rs370382506
|
0.00005
|
NM_001374353.1(GLI2):c.4241C>T (p.Pro1414Leu)
|
rs749402521
|
0.00005
|
NM_001374353.1(GLI2):c.2006C>T (p.Thr669Met)
|
rs758298657
|
0.00004
|
NM_001374353.1(GLI2):c.2089G>A (p.Ala697Thr)
|
rs553780090
|
0.00004
|
NM_001374353.1(GLI2):c.606C>T (p.Ser202=)
|
rs146181686
|
0.00004
|
NM_001374353.1(GLI2):c.1121G>A (p.Arg374His)
|
rs370220133
|
0.00003
|
NM_001374353.1(GLI2):c.2503G>A (p.Ala835Thr)
|
rs751028726
|
0.00003
|
NM_001374353.1(GLI2):c.4100G>A (p.Arg1367His)
|
rs763852684
|
0.00003
|
NM_001374353.1(GLI2):c.1481C>T (p.Ser494Leu)
|
rs372925840
|
0.00002
|
NM_001374353.1(GLI2):c.2075T>C (p.Leu692Pro)
|
rs781438228
|
0.00002
|
NM_001374353.1(GLI2):c.451G>A (p.Ala151Thr)
|
rs781771721
|
0.00002
|
NM_001374353.1(GLI2):c.196A>G (p.Met66Val)
|
rs768282760
|
0.00001
|
NM_001374353.1(GLI2):c.2208G>A (p.Thr736=)
|
rs372206751
|
0.00001
|
NM_001374353.1(GLI2):c.2657C>G (p.Thr886Ser)
|
rs572826436
|
0.00001
|
NM_001374353.1(GLI2):c.2690G>A (p.Arg897Gln)
|
rs886054813
|
0.00001
|
NM_001374353.1(GLI2):c.2884C>T (p.Leu962=)
|
rs1345329176
|
0.00001
|
NM_001374353.1(GLI2):c.3066C>T (p.Ala1022=)
|
rs1472557461
|
0.00001
|
NM_001374353.1(GLI2):c.314C>T (p.Pro105Leu)
|
rs370693310
|
0.00001
|
NM_001374353.1(GLI2):c.3784C>A (p.His1262Asn)
|
rs794727100
|
0.00001
|
NM_001374353.1(GLI2):c.765G>A (p.Ser255=)
|
rs200901345
|
0.00001
|
NM_001374353.1(GLI2):c.879C>T (p.Pro293=)
|
rs1318325355
|
0.00001
|
NM_001374353.1(GLI2):c.1125C>T (p.Ser375=)
|
rs1553475192
|
|
NM_001374353.1(GLI2):c.1370G>A (p.Trp457Ter)
|
rs1553476382
|
|
NM_001374353.1(GLI2):c.2136C>A (p.Phe712Leu)
|
rs151179617
|
|
NM_001374353.1(GLI2):c.2415C>T (p.Arg805=)
|
rs886044110
|
|
NM_001374353.1(GLI2):c.2748_2794del (p.Leu918fs)
|
rs1558941490
|
|
NM_001374353.1(GLI2):c.3037A>G (p.Ser1013Gly)
|
rs1553479006
|
|
NM_001374353.1(GLI2):c.3418C>T (p.Leu1140=)
|
rs141988240
|
|