List of variants reported as benign for Gonadotropin-independent familial sexual precocity by Illumina Laboratory Services, Illumina

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

Total variants: 30

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000233.4(LHCGR):c.866+8G>A	rs6755901	0.81104
NM_000233.4(LHCGR):c.1065T>C (p.Asp355=)	rs11125179	0.51451
NM_000233.4(LHCGR):c.935A>G (p.Asn312Ser)	rs2293275	0.51043
NM_000233.4(LHCGR):c.*221G>C	rs62137532	0.19256
NM_000233.3(LHCGR):c.-58G>T	rs10176989	0.18447
NM_000233.4(LHCGR):c.*148T>C	rs79248442	0.10655
NM_000233.4(LHCGR):c.*360G>A	rs10495956	0.04668
NM_000233.4(LHCGR):c.*528T>C	rs73928203	0.04337
NM_000233.4(LHCGR):c.872A>G (p.Asn291Ser)	rs12470652	0.03897
NM_000233.4(LHCGR):c.*131C>T	rs73928204	0.00766
NM_000233.4(LHCGR):c.1010T>C (p.Leu337Ser)	rs61996314	0.00677
NM_000233.4(LHCGR):c.622G>A (p.Val208Ile)	rs61996321	0.00614
NM_000233.4(LHCGR):c.606-5C>T	rs78135094	0.00306
NM_000233.4(LHCGR):c.458+3A>G	rs76210637	0.00257
NM_000233.4(LHCGR):c.*535G>A	rs534109670	0.00194
NM_000233.4(LHCGR):c.*22T>G	rs192235905	0.00152
NM_000233.4(LHCGR):c.1360G>A (p.Val454Ile)	rs114320052	0.00116
NM_000233.4(LHCGR):c.1953T>C (p.Tyr651=)	rs61996315	0.00075
NM_000233.4(LHCGR):c.371G>A (p.Arg124Gln)	rs140788691	0.00041
NM_000233.4(LHCGR):c.161+9A>G	rs573699597	0.00031
NM_000233.4(LHCGR):c.*7C>T	rs200256443	0.00029
NM_000233.4(LHCGR):c.561A>G (p.Glu187=)	rs369601921	0.00028
NM_000233.4(LHCGR):c.672G>A (p.Pro224=)	rs267599401	0.00016
NM_000233.4(LHCGR):c.707C>T (p.Ala236Val)	rs140148170	0.00014
NM_000233.4(LHCGR):c.681-6G>A	rs575168674	0.00006
NM_000233.4(LHCGR):c.1669G>A (p.Glu557Lys)	rs146785679	0.00005
NM_000233.4(LHCGR):c.1875A>T (p.Ile625=)	rs200691173	0.00005
NM_000233.4(LHCGR):c.*512C>T	rs564632841
NM_000233.4(LHCGR):c.337T>A (p.Tyr113Asn)	rs140691492
NM_000233.4(LHCGR):c.50_55dup (p.Gln18_Pro19insLeuGln)	rs71245621

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.