ClinVar Miner

List of variants reported as uncertain significance for X-linked disease by Genomic Medicine Lab, University of California San Francisco

Included ClinVar conditions (313):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 4
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HGVS dbSNP
NM_000047.3(ARSL):c.898G>A (p.Val300Ile) rs752354785
NM_001111125.3(IQSEC2):c.2894T>C (p.Leu965Pro) rs1602268775
NM_001111125.3(IQSEC2):c.808C>T (p.Arg270Trp) rs1602293814
NM_002968.2(SALL1):c.602A>G (p.Gln201Arg) rs775143619

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