ClinVar Miner

List of variants reported as uncertain significance for Leydig cell hypoplasia by Illumina Clinical Services Laboratory,Illumina

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 7
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HGVS dbSNP
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.*724T>C rs886056145
NM_000233.4(LHCGR):c.384-15T>C rs753540458
NM_000233.4(LHCGR):c.54G>A (p.Gln18=) rs780848944
NM_000233.4(LHCGR):c.811G>A (p.Ala271Thr) rs886056147

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