ClinVar Miner

List of variants reported as uncertain significance for Leydig cell hypoplasia, type 1

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Total variants: 37
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HGVS dbSNP
NM_000233.4(LHCGR):c.*182T>C
NM_000233.4(LHCGR):c.*192T>C
NM_000233.4(LHCGR):c.*273T>C rs886056146
NM_000233.4(LHCGR):c.*300T>A rs771456886
NM_000233.4(LHCGR):c.*383C>A rs777978092
NM_000233.4(LHCGR):c.*414T>C
NM_000233.4(LHCGR):c.*443C>T
NM_000233.4(LHCGR):c.*512C>T
NM_000233.4(LHCGR):c.*553A>T
NM_000233.4(LHCGR):c.*577T>A rs542577446
NM_000233.4(LHCGR):c.*710A>G
NM_000233.4(LHCGR):c.*724T>C rs886056145
NM_000233.4(LHCGR):c.*747C>A
NM_000233.4(LHCGR):c.*7C>T rs200256443
NM_000233.4(LHCGR):c.*805A>G
NM_000233.4(LHCGR):c.*894G>T
NM_000233.4(LHCGR):c.-32C>G
NM_000233.4(LHCGR):c.1308G>A (p.Gly436=)
NM_000233.4(LHCGR):c.132C>T (p.Cys44=)
NM_000233.4(LHCGR):c.1375G>A (p.Val459Ile)
NM_000233.4(LHCGR):c.161+9A>G
NM_000233.4(LHCGR):c.1752T>C (p.Pro584=)
NM_000233.4(LHCGR):c.1953T>C (p.Tyr651=) rs61996315
NM_000233.4(LHCGR):c.2002A>C (p.Thr668Pro) rs199807908
NM_000233.4(LHCGR):c.2072T>C (p.Leu691Pro)
NM_000233.4(LHCGR):c.2091A>T (p.Thr697=) rs148244033
NM_000233.4(LHCGR):c.2095T>A (p.Cys699Ser)
NM_000233.4(LHCGR):c.337T>A (p.Tyr113Asn) rs140691492
NM_000233.4(LHCGR):c.348C>T (p.Pro116=)
NM_000233.4(LHCGR):c.371G>A (p.Arg124Gln)
NM_000233.4(LHCGR):c.384-15T>C rs753540458
NM_000233.4(LHCGR):c.54G>A (p.Gln18=) rs780848944
NM_000233.4(LHCGR):c.561A>G (p.Glu187=) rs369601921
NM_000233.4(LHCGR):c.672G>A (p.Pro224=)
NM_000233.4(LHCGR):c.681-6G>A
NM_000233.4(LHCGR):c.707C>T (p.Ala236Val)
NM_000233.4(LHCGR):c.811G>A (p.Ala271Thr) rs886056147

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