ClinVar Miner

List of variants in gene combination LHCGR, STON1-GTF2A1L reported as benign for Leydig cell hypoplasia

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
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HGVS dbSNP
NM_000233.4(LHCGR):c.*148T>C rs79248442
NM_000233.4(LHCGR):c.*221G>C rs62137532
NM_000233.4(LHCGR):c.*360G>A rs10495956
NM_000233.4(LHCGR):c.*528T>C rs73928203
NM_000233.4(LHCGR):c.1065T>C (p.Asp355=) rs11125179
NM_000233.4(LHCGR):c.50_55dup (p.Leu17_Gln18dup) rs71245621
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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