ClinVar Miner

List of variants in gene LIFR reported as benign for Stüve-Wiedemann syndrome

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 54
Download table as spreadsheet
HGVS dbSNP
NM_001127671.2(LIFR):c.*1005A>G rs3776424
NM_001127671.2(LIFR):c.*1459T>G rs75965322
NM_001127671.2(LIFR):c.*1470T>G rs13156520
NM_001127671.2(LIFR):c.*1484A>G rs75368466
NM_001127671.2(LIFR):c.*1554C>G rs1428604
NM_001127671.2(LIFR):c.*1610T>G rs2731964
NM_001127671.2(LIFR):c.*1840C>G
NM_001127671.2(LIFR):c.*1870G>A rs60287085
NM_001127671.2(LIFR):c.*324G>A rs3797156
NM_001127671.2(LIFR):c.*3330C>A
NM_001127671.2(LIFR):c.*362G>A rs1005017
NM_001127671.2(LIFR):c.*3639_*3640del rs796517933
NM_001127671.2(LIFR):c.*3834C>G rs34130318
NM_001127671.2(LIFR):c.*394C>A rs115958115
NM_001127671.2(LIFR):c.*4056G>T rs73077449
NM_001127671.2(LIFR):c.*4243A>G rs73749255
NM_001127671.2(LIFR):c.*426G>A
NM_001127671.2(LIFR):c.*4804C>T rs55917124
NM_001127671.2(LIFR):c.*4854A>G rs35853268
NM_001127671.2(LIFR):c.*5072dup rs34579169
NM_001127671.2(LIFR):c.*5169T>A rs3822426
NM_001127671.2(LIFR):c.*5225C>T rs58755763
NM_001127671.2(LIFR):c.*5356A>G rs7713531
NM_001127671.2(LIFR):c.*546A>C rs3822427
NM_001127671.2(LIFR):c.*5634T>C rs149932478
NM_001127671.2(LIFR):c.*5670A>G rs3822425
NM_001127671.2(LIFR):c.*586A>T rs2561819
NM_001127671.2(LIFR):c.*6140C>G rs73077446
NM_001127671.2(LIFR):c.*6190C>T rs1046224
NM_001127671.2(LIFR):c.*6316C>T rs115572283
NM_001127671.2(LIFR):c.*988G>A rs3776425
NM_001127671.2(LIFR):c.143-11_143-10insGTGT rs1580121589
NM_001127671.2(LIFR):c.143-37GT[11] rs10637374
NM_001127671.2(LIFR):c.143-37GT[13] rs10637374
NM_001127671.2(LIFR):c.143-60A>G rs62355821
NM_001127671.2(LIFR):c.1732G>A (p.Asp578Asn) rs3729740
NM_001127671.2(LIFR):c.1886-18C>T rs3729743
NM_001127671.2(LIFR):c.1899A>G (p.Ile633Met) rs2303743
NM_001127671.2(LIFR):c.1915A>T (p.Met639Leu) rs143808825
NM_001127671.2(LIFR):c.1937C>A (p.Thr646Asn) rs79040751
NM_001127671.2(LIFR):c.1991C>T (p.Ser664Leu) rs3729744
NM_001127671.2(LIFR):c.2066-74T>G rs113874922
NM_001127671.2(LIFR):c.2302A>G (p.Arg768Gly) rs139848756
NM_001127671.2(LIFR):c.2353G>A (p.Val785Ile) rs3110234
NM_001127671.2(LIFR):c.2498-7G>A rs113078097
NM_001127671.2(LIFR):c.2578C>T (p.Arg860Trp) rs146205670
NM_001127671.2(LIFR):c.2766T>C (p.Asp922=) rs61027880
NM_001127671.2(LIFR):c.3288C>T (p.Asn1096=) rs3729751
NM_001127671.2(LIFR):c.346C>T (p.His116Tyr) rs3729734
NM_001127671.2(LIFR):c.397+17_397+20del rs139143276
NM_001127671.2(LIFR):c.789A>G (p.Val263=) rs141925289
NM_001127671.2(LIFR):c.954C>T (p.Thr318=) rs61748202
NM_001127671.2(LIFR):c.991+80G>T rs6451387
NM_002310.6(LIFR):c.-20+294A>T rs186528221

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.