ClinVar Miner

List of variants reported as likely pathogenic for congenital hypogonadotropic hypogonadism by Institute of Medical Genetics and Genomics, Sir Ganga Ram Hospital

Included ClinVar conditions (68):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_000475.5(NR0B1):c.1006dup (p.Val336fs) rs1926565039
NM_178138.6(LHX3):c.581C>G (p.Thr194Arg) rs2131032901

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