ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 82
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001127671.2(LIFR):c.2671-184G>A rs2256595 0.46511
NM_001127671.2(LIFR):c.397+29A>C rs2289779 0.37791
NM_001127671.2(LIFR):c.562-88A>G rs1037033 0.30225
NM_001127671.2(LIFR):c.561+216A>G rs1822815 0.30148
NM_001127671.2(LIFR):c.1292-80T>A rs16903989 0.29875
NM_001127671.2(LIFR):c.1672-82G>A rs3729741 0.29783
NM_001127671.2(LIFR):c.1885+222A>G rs2162885 0.29596
NM_001127671.2(LIFR):c.2353G>A (p.Val785Ile) rs3110234 0.17829
NM_001127671.2(LIFR):c.2167+21T>C rs3110971 0.17819
NM_001127671.2(LIFR):c.398-56A>G rs3729598 0.06976
NM_001127671.2(LIFR):c.2065+142C>T rs62353655 0.04077
NM_001127671.2(LIFR):c.143-60A>G rs62355821 0.04013
NM_001127671.2(LIFR):c.1672-148C>T rs2561826 0.04005
NM_001127671.2(LIFR):c.1672-180C>T rs2561827 0.03991
NM_001127671.2(LIFR):c.346C>T (p.His116Tyr) rs3729734 0.03927
NM_001127671.2(LIFR):c.2671-158_2671-157insTTTT rs1278539486 0.03440
NM_001127671.2(LIFR):c.2671-149_2671-148insTCCG rs1437530857 0.03436
NM_001127671.2(LIFR):c.2671-152del rs1220261200 0.03436
NM_001127671.2(LIFR):c.2671-150A>T rs1338198293 0.03435
NM_001127671.2(LIFR):c.2671-143_2671-119del rs1405234004 0.03427
NM_001127671.2(LIFR):c.991+80G>T rs6451387 0.03281
NM_001127671.2(LIFR):c.2498-243G>T rs75261849 0.03256
NM_001127671.2(LIFR):c.258-132G>A rs16903991 0.03242
NM_001127671.2(LIFR):c.1438-117G>A rs7701409 0.02036
NM_001127671.2(LIFR):c.992-246A>G rs73749259 0.01934
NM_001127671.2(LIFR):c.1291+252A>G rs58036502 0.01744
NM_001127671.2(LIFR):c.1671+261T>C rs11956342 0.01543
NM_001127671.2(LIFR):c.1886-18C>T rs3729743 0.01528
NM_001127671.2(LIFR):c.1937C>A (p.Thr646Asn) rs79040751 0.00875
NM_001127671.2(LIFR):c.1732G>A (p.Asp578Asn) rs3729740 0.00852
NM_001127671.2(LIFR):c.1899A>G (p.Ile633Met) rs2303743 0.00702
NM_001127671.2(LIFR):c.1991C>T (p.Ser664Leu) rs3729744 0.00642
NM_001127671.2(LIFR):c.2766T>C (p.Asp922=) rs61027880 0.00501
NM_001127671.2(LIFR):c.2591+17T>C rs73077453 0.00459
NM_001127671.2(LIFR):c.954C>T (p.Thr318=) rs61748202 0.00421
NM_001127671.2(LIFR):c.420G>A (p.Glu140=) rs142475175 0.00380
NM_001127671.2(LIFR):c.789A>G (p.Val263=) rs141925289 0.00321
NM_001127671.2(LIFR):c.2498-7G>A rs113078097 0.00306
NM_001127671.2(LIFR):c.2447A>G (p.Asp816Gly) rs74856317 0.00245
NM_001127671.2(LIFR):c.2578C>T (p.Arg860Trp) rs146205670 0.00066
NM_001127671.2(LIFR):c.1915A>T (p.Met639Leu) rs143808825 0.00064
NM_001127671.2(LIFR):c.774T>C (p.Asp258=) rs761633332 0.00016
NM_001127671.2(LIFR):c.1722G>A (p.Ser574=) rs200521119 0.00008
NM_001127671.2(LIFR):c.2497+14T>G rs541984532 0.00004
NM_001127671.2(LIFR):c.3060G>A (p.Glu1020=) rs537706381 0.00001
GRCh37/hg19 5p13.1(chr5:38536315-38556894)x1
GRCh37/hg19 5p13.1(chr5:38536315-38556970)x1
GRCh37/hg19 5p13.1(chr5:38556294-38556650)x1
GRCh37/hg19 5p13.1(chr5:38556294-38556694)x1
GRCh37/hg19 5p13.1(chr5:38556294-38556706)x1
GRCh37/hg19 5p13.1(chr5:38556294-38556894)x1
GRCh37/hg19 5p13.1(chr5:38556294-38556970)x1
GRCh37/hg19 5p13.1(chr5:38556294-38557021)x1
GRCh37/hg19 5p13.1(chr5:38556345-38557021)x1
GRCh37/hg19 5p13.1(chr5:38556594-38556706)x1
GRCh37/hg19 5p13.1(chr5:38556594-38556894)x1
NM_001127671.2(LIFR):c.1292-19_1292-18del rs564274522
NM_001127671.2(LIFR):c.1417T>C (p.Ser473Pro) rs543824186
NM_001127671.2(LIFR):c.142+122del rs11293177
NM_001127671.2(LIFR):c.143-37GT[10] rs10637374
NM_001127671.2(LIFR):c.143-37GT[12] rs10637374
NM_001127671.2(LIFR):c.143-37GT[13] rs10637374
NM_001127671.2(LIFR):c.143-37GT[15] rs10637374
NM_001127671.2(LIFR):c.143-37GT[16] rs10637374
NM_001127671.2(LIFR):c.143-37GT[17] rs10637374
NM_001127671.2(LIFR):c.143-39_143-28del rs3836782
NM_001127671.2(LIFR):c.143-5_143-3del rs778581246
NM_001127671.2(LIFR):c.1600+17A>G
NM_001127671.2(LIFR):c.1601-3del rs776524743
NM_001127671.2(LIFR):c.1671+18C>T
NM_001127671.2(LIFR):c.2336-4dup rs2112378006
NM_001127671.2(LIFR):c.2592-9del
NM_001127671.2(LIFR):c.2671-162T>G rs573391870
NM_001127671.2(LIFR):c.3288C>T (p.Asn1096=) rs3729751
NM_001127671.2(LIFR):c.397+17_397+20del rs139143276
NM_001127671.2(LIFR):c.561+212G>A rs7727565
NM_001127671.2(LIFR):c.562-3del
NM_001127671.2(LIFR):c.737-13dup rs2112493883
NM_001127671.2(LIFR):c.737-15T>C
NM_001127671.2(LIFR):c.991+84del rs34968906
NM_001127671.2(LIFR):c.992-8del
NM_001127671.2(LIFR):c.992-8dup rs773048780

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.