ClinVar Miner

Submissions for variant NM_002256.4(KISS1):c.283C>T (p.Pro95Ser)

gnomAD frequency: 0.00004  dbSNP: rs777274044
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ulrich Schweizer laboratory, Universitaetsklinikum Bonn RCV002273838 SCV002098392 uncertain significance Disorder of sexual differentiation 2021-09-01 no assertion criteria provided clinical testing

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