List of variants in gene LHB studied for Isolated lutropin deficiency

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000894.3(LHB):c.285T>C (p.Gly95=)	rs1056917	0.65129
NM_000894.3(LHB):c.183+11T>C	rs2387588	0.63010
NM_000894.3(LHB):c.183+18del	rs140502544	0.62955
NM_000894.3(LHB):c.16-26T>C	rs4002462	0.62429
NM_000894.3(LHB):c.132A>C (p.Pro44=)	rs1056914	0.55157
NM_000894.3(LHB):c.114C>G (p.Val38=)	rs6521	0.54755
NM_000894.3(LHB):c.15+9A>G	rs2387589	0.47035
NM_000894.3(LHB):c.233C>A (p.Thr78Asn)	rs116437960	0.01395
NM_000894.3(LHB):c.364G>A (p.Gly122Ser)	rs5030774	0.00030
NM_000894.3(LHB):c.286G>A (p.Val96Met)	rs149003040	0.00016
NM_000894.3(LHB):c.167G>A (p.Gly56Asp)	rs121912517	0.00005
NM_000894.3(LHB):c.183+1G>C	rs786204822
NM_000894.3(LHB):c.183+1G>T	rs786204822
NM_000894.3(LHB):c.221A>G (p.Gln74Arg)	rs5030773
NM_000894.3(LHB):c.28_39del (p.Leu10_Leu13del)	rs769066903
NM_000894.3(LHB):c.88_96del (p.His30_Ile32del)	rs786204823

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