List of variants in gene LIFR reported as likely benign for bone disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 41

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HGVS	dbSNP	gnomAD frequency
NM_001127671.2(LIFR):c.*6640dup	rs57386567	0.04372
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.789A>G (p.Val263=)	rs141925289	0.00321
NM_001127671.2(LIFR):c.2498-7G>A	rs113078097	0.00306
NM_001127671.2(LIFR):c.*2570G>C	rs113730751	0.00296
NM_001127671.2(LIFR):c.*2567G>A	rs112458059	0.00295
NM_001127671.2(LIFR):c.*5125C>T	rs147202739	0.00270
NM_001127671.2(LIFR):c.2447A>G (p.Asp816Gly)	rs74856317	0.00245
NM_001127671.2(LIFR):c.*398C>G	rs138772371	0.00240
NM_001127671.2(LIFR):c.2302A>G (p.Arg768Gly)	rs139848756	0.00107
NM_001127671.2(LIFR):c.2934G>A (p.Gln978=)	rs148354076	0.00082
NM_001127671.2(LIFR):c.*2712C>T	rs547688841	0.00063
NM_001127671.2(LIFR):c.3087A>G (p.Arg1029=)	rs138418444	0.00055
NM_001127671.2(LIFR):c.2280G>A (p.Leu760=)	rs370455274	0.00010
NM_001127671.2(LIFR):c.2886C>T (p.Ala962=)	rs775970749	0.00010
NM_001127671.2(LIFR):c.2591+6A>T	rs372291945	0.00009
NM_001127671.2(LIFR):c.1722G>A (p.Ser574=)	rs200521119	0.00008
NM_001127671.2(LIFR):c.2463G>A (p.Pro821=)	rs749085598	0.00008
NM_001127671.2(LIFR):c.*3851T>A	rs78474283	0.00006
NM_001127671.2(LIFR):c.147T>G (p.Ala49=)	rs879807300	0.00005
NM_001127671.2(LIFR):c.2529A>G (p.Pro843=)	rs779533679	0.00005
NM_001127671.2(LIFR):c.1080G>A (p.Ala360=)	rs769294023	0.00004
NM_001127671.2(LIFR):c.1974C>T (p.Val658=)	rs762685098	0.00004
NM_001127671.2(LIFR):c.2217G>A (p.Ser739=)	rs747295716	0.00004
NM_001127671.2(LIFR):c.2497+14T>G	rs541984532	0.00004
NM_001127671.2(LIFR):c.1221T>C (p.Asn407=)	rs372077841	0.00003
NM_001127671.2(LIFR):c.15C>T (p.Tyr5=)	rs778287994	0.00003
NM_001127671.2(LIFR):c.2670+6C>G	rs898718526	0.00003
NM_001127671.2(LIFR):c.552C>T (p.Leu184=)	rs370454146	0.00002
NM_001127671.2(LIFR):c.2910A>G (p.Ala970=)	rs1258728953	0.00001
NM_001127671.2(LIFR):c.3060G>A (p.Glu1020=)	rs537706381	0.00001
NM_001127671.2(LIFR):c.819T>C (p.Ser273=)	rs756161883	0.00001
NM_001127671.2(LIFR):c.*4154A>G	rs73077448
NM_001127671.2(LIFR):c.1245G>A (p.Pro415=)	rs139809889
NM_001127671.2(LIFR):c.1365A>G (p.Leu455=)	rs1204654428
NM_001127671.2(LIFR):c.143-5_143-3del	rs778581246
NM_001127671.2(LIFR):c.194G>C (p.Cys65Ser)
NM_001127671.2(LIFR):c.3288C>A (p.Asn1096Lys)	rs3729751
NM_001127671.2(LIFR):c.3288C>T (p.Asn1096=)	rs3729751
NM_001127671.2(LIFR):c.33A>G (p.Pro11=)

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