ClinVar Miner

List of variants in gene S1PR2 reported as pathogenic for autosomal recessive nonsyndromic deafness 68

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 2
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NM_004230.4(S1PR2):c.323G>C (p.Arg108Pro) rs869312749
NM_004230.4(S1PR2):c.419A>G (p.Tyr140Cys) rs869312750

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