ClinVar Miner

List of variants in gene FTO reported as uncertain significance for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 52
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001080432.3(FTO):c.601G>A (p.Val201Ile) rs150450891 0.00058
NM_001080432.3(FTO):c.1198A>G (p.Met400Val) rs143788264 0.00043
NM_001080432.3(FTO):c.428A>G (p.Asn143Ser) rs147561986 0.00039
NM_001080432.3(FTO):c.1081C>T (p.Pro361Ser) rs369714221 0.00021
NM_001080432.3(FTO):c.436C>A (p.Leu146Met) rs182784714 0.00021
NM_001080432.3(FTO):c.238C>T (p.Arg80Trp) rs140101381 0.00017
NM_001080432.3(FTO):c.1017G>T (p.Gln339His) rs200895945 0.00013
NM_001080432.3(FTO):c.1465C>T (p.Leu489Phe) rs370137051 0.00010
NM_001080432.3(FTO):c.1474A>G (p.Ile492Val) rs373102373 0.00010
NM_001080432.3(FTO):c.1274G>T (p.Gly425Val) rs376527078 0.00009
NM_001080432.3(FTO):c.857C>T (p.Ala286Val) rs370075174 0.00009
NM_001080432.3(FTO):c.185A>G (p.His62Arg) rs550932456 0.00008
NM_001080432.3(FTO):c.1295A>G (p.Asn432Ser) rs141327394 0.00004
NM_001080432.3(FTO):c.1418G>A (p.Arg473Gln) rs777486753 0.00004
NM_001080432.3(FTO):c.793A>G (p.Arg265Gly) rs756019558 0.00004
NM_001080432.3(FTO):c.667A>G (p.Met223Val) rs780601119 0.00003
NM_001080432.3(FTO):c.1365G>T (p.Arg455Ser) rs376381270 0.00002
NM_001080432.3(FTO):c.1282G>A (p.Val428Met) rs371704660 0.00001
NM_001080432.3(FTO):c.154C>T (p.Arg52Ter) rs531215275 0.00001
NM_001080432.3(FTO):c.785T>C (p.Leu262Pro) rs148528422 0.00001
NM_001080432.3(FTO):c.931G>T (p.Ala311Ser) rs200152693 0.00001
NM_001080432.3(FTO):c.946C>T (p.Arg316Trp) rs777196899 0.00001
NM_001080432.3(FTO):c.998A>G (p.Tyr333Cys) rs781481485 0.00001
GRCh37/hg19 16q12.2(chr16:53906098-54003147)x1
NC_000016.9:g.(?_53907678)_(53922883_?)del
NM_001080432.3(FTO):c.10A>G (p.Thr4Ala) rs752817421
NM_001080432.3(FTO):c.1195C>T (p.Pro399Ser)
NM_001080432.3(FTO):c.1239+6T>C
NM_001080432.3(FTO):c.1261G>T (p.Val421Phe)
NM_001080432.3(FTO):c.1276C>G (p.Leu426Val) rs576410322
NM_001080432.3(FTO):c.1293G>C (p.Arg431Ser)
NM_001080432.3(FTO):c.1393C>T (p.Pro465Ser)
NM_001080432.3(FTO):c.1448_1463dup (p.Asp488_Leu489insAlaSerAlaValTer)
NM_001080432.3(FTO):c.1475T>C (p.Ile492Thr)
NM_001080432.3(FTO):c.189A>T (p.Lys63Asn)
NM_001080432.3(FTO):c.252G>C (p.Arg84Ser)
NM_001080432.3(FTO):c.257A>G (p.Gln86Arg) rs778585710
NM_001080432.3(FTO):c.278C>G (p.Pro93Arg) rs151263395
NM_001080432.3(FTO):c.286C>T (p.Arg96Cys)
NM_001080432.3(FTO):c.287G>A (p.Arg96His) rs139577103
NM_001080432.3(FTO):c.442A>G (p.Ile148Val) rs2151775451
NM_001080432.3(FTO):c.754C>T (p.Pro252Ser) rs2079552258
NM_001080432.3(FTO):c.791G>A (p.Gly264Asp)
NM_001080432.3(FTO):c.809G>A (p.Trp270Ter)
NM_001080432.3(FTO):c.86C>T (p.Pro29Leu)
NM_001080432.3(FTO):c.889A>G (p.Met297Val)
NM_001080432.3(FTO):c.88T>C (p.Tyr30His)
NM_001080432.3(FTO):c.899A>G (p.Asp300Gly) rs2151879431
NM_001080432.3(FTO):c.8G>C (p.Arg3Pro)
NM_001080432.3(FTO):c.914A>G (p.His305Arg)
NM_001080432.3(FTO):c.976T>C (p.Cys326Arg) rs779204175
NM_001080432.3(FTO):c.995A>C (p.Asp332Ala)

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.