List of variants in gene combination LHCGR, STON1-GTF2A1L reported as benign by Illumina Laboratory Services, Illumina

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: 30

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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.*528T>C	rs73928203	0.04337
NM_000233.4(LHCGR):c.*360G>A	rs10495956	0.04324
NM_000233.4(LHCGR):c.872A>G (p.Asn291Ser)	rs12470652	0.03749
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	0.00283
NM_000233.4(LHCGR):c.458+3A>G	rs76210637	0.00251
NM_000233.4(LHCGR):c.*535G>A	rs534109670	0.00191
NM_000233.4(LHCGR):c.*22T>G	rs192235905	0.00139
NM_000233.4(LHCGR):c.1360G>A (p.Val454Ile)	rs114320052	0.00116
NM_000233.4(LHCGR):c.1953T>C (p.Tyr651=)	rs61996315	0.00070
NM_000233.4(LHCGR):c.371G>A (p.Arg124Gln)	rs140788691	0.00036
NM_000233.4(LHCGR):c.*512C>T	rs564632841	0.00033
NM_000233.4(LHCGR):c.161+9A>G	rs573699597	0.00031
NM_000233.4(LHCGR):c.561A>G (p.Glu187=)	rs369601921	0.00027
NM_000233.4(LHCGR):c.*7C>T	rs200256443	0.00026
NM_000233.4(LHCGR):c.707C>T (p.Ala236Val)	rs140148170	0.00017
NM_000233.4(LHCGR):c.672G>A (p.Pro224=)	rs267599401	0.00015
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.337T>A (p.Tyr113Asn)	rs140691492
NM_000233.4(LHCGR):c.50_55dup (p.Gln18_Pro19insLeuGln)	rs71245621

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