ClinVar Miner

List of variants in gene LHCGR, STON1-GTF2A1L studied for Leydig cell hypoplasia

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 49
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HGVS dbSNP
NM_000233.4(LHCGR):c.*131C>T rs73928204
NM_000233.4(LHCGR):c.*148T>C rs79248442
NM_000233.4(LHCGR):c.*221G>C rs62137532
NM_000233.4(LHCGR):c.*273T>C rs886056146
NM_000233.4(LHCGR):c.*281del rs558291070
NM_000233.4(LHCGR):c.*300T>A rs771456886
NM_000233.4(LHCGR):c.*360G>A rs10495956
NM_000233.4(LHCGR):c.*383C>A rs777978092
NM_000233.4(LHCGR):c.*528T>C rs73928203
NM_000233.4(LHCGR):c.*535G>A rs534109670
NM_000233.4(LHCGR):c.*577T>A rs542577446
NM_000233.4(LHCGR):c.*724T>C rs886056145
NM_000233.4(LHCGR):c.*7C>T rs200256443
NM_000233.4(LHCGR):c.1010T>C (p.Leu337Ser) rs61996314
NM_000233.4(LHCGR):c.1027T>A (p.Cys343Ser) rs121912536
NM_000233.4(LHCGR):c.1060G>A (p.Glu354Lys) rs121912529
NM_000233.4(LHCGR):c.1065T>C (p.Asp355=) rs11125179
NM_000233.4(LHCGR):c.1360G>A (p.Val454Ile) rs114320052
NM_000233.4(LHCGR):c.1505T>C (p.Leu502Pro) rs121912538
NM_000233.4(LHCGR):c.1627T>C (p.Cys543Arg) rs121912537
NM_000233.4(LHCGR):c.1635C>A (p.Cys545Ter) rs121912523
NM_000233.4(LHCGR):c.1660C>T (p.Arg554Ter) rs121912524
NM_000233.4(LHCGR):c.1669G>A (p.Glu557Lys) rs146785679
NM_000233.4(LHCGR):c.1733A>G (p.Asp578Gly) rs121912518
NM_000233.4(LHCGR):c.1777G>C (p.Ala593Pro) rs121912520
NM_000233.4(LHCGR):c.1869T>G (p.Tyr623Ter) rs144859947
NM_000233.4(LHCGR):c.1874T>A (p.Ile625Lys) rs121912530
NM_000233.4(LHCGR):c.1875A>T (p.Ile625=) rs200691173
NM_000233.4(LHCGR):c.2002A>C (p.Thr668Pro) rs199807908
NM_000233.4(LHCGR):c.337T>A (p.Tyr113Asn) rs140691492
NM_000233.4(LHCGR):c.370C>T (p.Arg124Ter) rs773279269
NM_000233.4(LHCGR):c.378A>C (p.Lys126Asn) rs373456950
NM_000233.4(LHCGR):c.384-15T>C rs753540458
NM_000233.4(LHCGR):c.391T>C (p.Cys131Arg) rs121912527
NM_000233.4(LHCGR):c.430G>A (p.Val144Ile) rs121912539
NM_000233.4(LHCGR):c.430G>T (p.Val144Phe) rs121912539
NM_000233.4(LHCGR):c.442G>T (p.Glu148Ter) rs140568136
NM_000233.4(LHCGR):c.458+3A>G rs76210637
NM_000233.4(LHCGR):c.50_55dup (p.Leu17_Gln18dup) rs71245621
NM_000233.4(LHCGR):c.54G>A (p.Gln18=) rs780848944
NM_000233.4(LHCGR):c.606-5C>T rs78135094
NM_000233.4(LHCGR):c.610C>T (p.Leu204=) rs61996322
NM_000233.4(LHCGR):c.709del (p.Leu237fs) rs1553387851
NM_000233.4(LHCGR):c.811G>A (p.Ala271Thr) rs886056147
NM_000233.4(LHCGR):c.81G>A (p.Glu27=) rs527550554
NM_000233.4(LHCGR):c.866+8G>A rs6755901
NM_000233.4(LHCGR):c.872A>G (p.Asn291Ser) rs12470652
NM_000233.4(LHCGR):c.935A>G (p.Asn312Ser) rs2293275
NM_001198593.1(STON1-GTF2A1L):c.3442-20551C>A rs10176989

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