ClinVar Miner

List of variants in gene LIFR reported as benign for bone development disease

Included ClinVar conditions (618):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_001127671.2(LIFR):c.*362G>A rs1005017 0.70336
NM_001127671.2(LIFR):c.397+29A>C rs2289779 0.37791
NM_001127671.2(LIFR):c.*1470T>G rs13156520 0.30679
NM_001127671.2(LIFR):c.*5670A>G rs3822425 0.30662
NM_001127671.2(LIFR):c.*6190C>T rs1046224 0.30641
NM_001127671.2(LIFR):c.*3834C>G rs34130318 0.30347
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.*5169T>A rs3822426 0.18293
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.*586A>T rs2561819 0.10855
NM_001127671.2(LIFR):c.*4854A>G rs35853268 0.06740
NM_001127671.2(LIFR):c.*5356A>G rs7713531 0.04455
NM_001127671.2(LIFR):c.143-60A>G rs62355821 0.04013
NM_001127671.2(LIFR):c.346C>T (p.His116Tyr) rs3729734 0.03927
NM_001127671.2(LIFR):c.*5225C>T rs58755763 0.03718
NM_001127671.2(LIFR):c.*4243A>G rs73749255 0.03708
NM_001127671.2(LIFR):c.991+80G>T rs6451387 0.03281
NM_001127671.2(LIFR):c.*1554C>G rs1428604 0.02039
NM_001127671.2(LIFR):c.*4804C>T rs55917124 0.01942
NM_001127671.2(LIFR):c.*426G>A rs116625329 0.01616
NM_001127671.2(LIFR):c.*988G>A rs3776425 0.01550
NM_001127671.2(LIFR):c.*4056G>T rs73077449 0.01539
NM_001127671.2(LIFR):c.1886-18C>T rs3729743 0.01528
NM_001127671.2(LIFR):c.2066-74T>G rs113874922 0.01368
NM_001127671.2(LIFR):c.*6316C>T rs115572283 0.01333
NM_001127671.2(LIFR):c.*1610T>G rs2731964 0.01049
NM_001127671.2(LIFR):c.*1484A>G rs75368466 0.00893
NM_001127671.2(LIFR):c.1937C>A (p.Thr646Asn) rs79040751 0.00875
NM_001127671.2(LIFR):c.*394C>A rs115958115 0.00870
NM_001127671.2(LIFR):c.*546A>C rs3822427 0.00868
NM_001127671.2(LIFR):c.*1870G>A rs60287085 0.00865
NM_001127671.2(LIFR):c.*1459T>G rs75965322 0.00858
NM_001127671.2(LIFR):c.*324G>A rs3797156 0.00855
NM_001127671.2(LIFR):c.1732G>A (p.Asp578Asn) rs3729740 0.00852
NM_001127671.2(LIFR):c.*1005A>G rs3776424 0.00851
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.*6140C>G rs73077446 0.00501
NM_001127671.2(LIFR):c.2766T>C (p.Asp922=) rs61027880 0.00501
NM_001127671.2(LIFR):c.*5634T>C rs149932478 0.00490
NM_002310.6(LIFR):c.-20+294A>T rs186528221 0.00479
NM_001127671.2(LIFR):c.954C>T (p.Thr318=) rs61748202 0.00421
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.2302A>G (p.Arg768Gly) rs139848756 0.00107
NM_001127671.2(LIFR):c.3039G>C (p.Val1013=) rs754819659 0.00068
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.*1840C>G rs190209875 0.00053
NM_001127671.2(LIFR):c.774T>C (p.Asp258=) rs761633332 0.00016
NM_001127671.2(LIFR):c.143-39C>G rs62355820 0.00015
NM_001127671.2(LIFR):c.*3330C>A rs148827994
NM_001127671.2(LIFR):c.*3639_*3640del rs796517933
NM_001127671.2(LIFR):c.*5072dup rs34579169
NM_001127671.2(LIFR):c.143-37GT[11] 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.3288C>T (p.Asn1096=) rs3729751
NM_001127671.2(LIFR):c.397+17_397+20del rs139143276

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